PRP in ACLR to Prevent PTOA
Primary Purpose
Anterior Cruciate Ligament Injuries, Post-traumatic Osteoarthritis, PRP
Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
platelet rich plasma (PRP) injection
placebo saline injection
Sponsored by
About this trial
This is an interventional prevention trial for Anterior Cruciate Ligament Injuries focused on measuring platelet-rich plasma, regenerative medicine, anterior cruciate ligament reconstruction, post-traumatic osteoarthritis
Eligibility Criteria
Inclusion Criteria:
- Acute ACL injury within 6 weeks of presentation
- Age 14-50
- Male or female
- Meniscus injury that can be treated with meniscectomy or repair (the lack of meniscus injury will not exclude patients)
Exclusion Criteria:
- Prior ACL reconstruction
- Prior cartilage repair procedure
- Prior meniscus surgery within 12 months
- Prior steroid, hyaluronic acid, or PRP injection within 6 months
- Other ligament injury requiring repair
- Any cartilage lesion requiring repair
- Any cartilage lesion greater than grade 2 (partial thickness injury)
- History of inflammatory arthritis or joint sepsis
- Non English speakers
Sites / Locations
- Hospital for Special SurgeryRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Control Arm
Investigational Arm
Arm Description
The control arm will receive a pre-op placebo injection of saline, and ACLR surgery with intra-op placebo injection
The investigational arm will receive a pre-op PRP injection, and ACLR surgery with PRP injection
Outcomes
Primary Outcome Measures
Platelet count (Thousand/uL)
Platelet count (Thousand/uL) will be measured by completing a complete blood count on patient's blood sample.
Platelet count (Thousand/uL)
Platelet count (Thousand/uL) will be measured by completing a complete blood count on patient's blood sample.
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Numeric Pain Rating Scale (NPRS)
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Numeric Pain Rating Scale (NPRS)
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Numeric Pain Rating Scale (NPRS)
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Numeric Pain Rating Scale (NPRS)
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Numeric Pain Rating Scale (NPRS)
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Numeric Pain Rating Scale (NPRS)
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Single Assessment Numeric Evaluation (SANE)
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Single Assessment Numeric Evaluation (SANE)
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Single Assessment Numeric Evaluation (SANE)
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Single Assessment Numeric Evaluation (SANE)
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Single Assessment Numeric Evaluation (SANE)
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Single Assessment Numeric Evaluation (SANE)
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Single Assessment Numeric Evaluation (SANE)
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Secondary Outcome Measures
Knee stability
Using the KT1000 arthrometer
Knee stability
Using the KT1000 arthrometer
Knee stability
Using the KT1000 arthrometer
Knee strength
Using the Cybex test
Knee strength
Using the Cybex test
Knee strength
Using the Cybex test
Full Information
NCT ID
NCT05412381
First Posted
April 7, 2022
Last Updated
July 31, 2023
Sponsor
Hospital for Special Surgery, New York
Collaborators
Orthopedic Research and Education Foundation
1. Study Identification
Unique Protocol Identification Number
NCT05412381
Brief Title
PRP in ACLR to Prevent PTOA
Official Title
Platelet Rich Plasma (PRP) Treatment of the Anterior Cruciate Ligament Injured Knee to Decrease the Risk of Post-traumatic Osteoarthritis (PTOA): a Randomized Double-blind Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 27, 2022 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital for Special Surgery, New York
Collaborators
Orthopedic Research and Education Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of our study is to examine the effect of platelet-rich-plasma (PRP) injection on the short-term resolution of post-injury inflammation (biomarkers) and improvement in joint function in patients with acute ACL injury. This RCT has been powered based on the questionnaire KOOS Jr. but it is considered a 'pilot study' in terms of the lab analysis proposed.
Detailed Description
Anterior cruciate ligament (ACL) injury is one of the most common clinical problems among active individuals, with over 250,000 ACL reconstructions (ACLR) per year in the United States. Surgical reconstruction of the ACL is typically required in individuals who wish to return to an active lifestyle due to the presence of knee instability. The results of ACLR are predictably good as far as the ability to re-establish knee stability and to allow return to cutting and pivoting activities. However, there is a lack of effective interventions that can successfully delay or prevent the progressive degenerative changes that are known to occur following injury and that will ultimately lead to post-traumatic osteoarthritis (PTOA). PTOA accounts for nearly 12% of all cases of symptomatic OA, or approximately 5.6 million cases of lower extremity OA in the United States, carrying a cost of over $11.8 billion annually. As injury rates rise and PTOA becomes more prevalent, the associated socioeconomic burden is a significant concern since these injuries have a particularly high incidence in young adults. Many different factors likely contribute to the development of PTOA following ACLR, including the inflammatory response that occurs following injury, altered knee kinematics that can persist despite "successful" ACLR, and persistent deficits in strength of the muscles around the knee. It is well-accepted that the accumulation of inflammatory mediators and matrix degrading proteases that occurs following joint injury likely plays an important role in the initiation of the pathological process leading to PTOA. Work in animal models shows that synovial inflammation plays a central role in the development of PTOA, and studies in patients undergoing ACLR uncovered synovial fluid biomarkers with prognostic value and showed that treatment with anti-inflammatory agents modulated biomarkers of cartilage degeneration. Our preliminary RNA-seq in synovial biopsies from patients undergoing arthroscopic ACLR revealed time-dependent changes in the inflammatory gene expression profile of these tissues, further suggesting that preventative therapies that dampen inflammation early after injury and before surgery may contribute to prevent the onset of PTOA. Abnormalities in the infrapatellar fat pad (IFP) are also associated with higher inflammatory synovial fluid cytokine profile following ACL tear, highlighting the contribution of the IFP-synovial compartment to the inflammatory burden of the knee. In addition to the inflammatory response that occurs following injury, inflammation also occurs following surgery. This "double hit" may play an important role in the development of PTOA, suggesting that methods to ameliorate the inflammatory process following joint injury could represent an effective therapeutic strategy.
The current standard methods available to clinicians to treat joint inflammation include oral non-steroidal anti-inflammatory (NSAID) medications and corticosteroid injection. However, clinicians have begun to use "orthobiologics" more frequently due to their potential to diminish inflammatory and catabolic mediators while also promoting repair, and because its autologous and minimally manipulated nature is not subjected to pre-market regulatory clearance from the Food and Drug Administration. Platelet rich plasma (PRP) is a non-surgical therapy increasingly used as an alternative to NSAIDs. PRP contains and releases a wide array of bioactive molecules it has been used to treat bone, tendon, and ligament injuries, and has emerged as a potential treatment for knee osteoarthritis (OA). The currently available studies comparing intra-articular PRP injections to other means of non-surgical intervention for knee OA report promising results with the use of PRP. These data suggest that positive clinical results in OA patients are mainly related to the immune modulatory effects of PRP, dampening the intra-articular inflammatory responses.
However, the role of PRP in the treatment of knee OA remains inconclusive, largely due to inconsistencies and high variability in PRP preparations, and the limited information about the relevant components in PRP that impact clinical responses. Factors including age, sex, medical comorbidities, and genetic profile may affect the composition and biologic activity of PRP samples derived from different individuals. In addition to inter-individual variations, there is currently very little data to define how the composition and biologic activity of PRP relates to the clinical outcomes. Our recent pilot data suggests that, indeed, there are changes in composition and PRP bioactivity that may be associated with variable clinical outcomes in patients with established knee OA receiving intra-articular PRP injections. However, larger clinical trials are still required to better define these changes and to establish truly mechanistic and functional correlations. Thus, a large knowledge gap remains in our understanding of the biologically active components of PRP. Furthermore, the limited data available related to PRP and knee OA addresses treatment of established OA. There is no information available about the potential of PRP for prevention of the pathological cascade leading to PTOA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Injuries, Post-traumatic Osteoarthritis, PRP
Keywords
platelet-rich plasma, regenerative medicine, anterior cruciate ligament reconstruction, post-traumatic osteoarthritis
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
PRP is considered a biologic.
We designed a double-blinded randomized controlled clinical trial with two arms:
Control Arm (pre-op placebo injection, ACLR surgery + placebo injection)
Investigational Arm (pre-op PRP injection, ACLR surgery + PRP injection).
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
56 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control Arm
Arm Type
Placebo Comparator
Arm Description
The control arm will receive a pre-op placebo injection of saline, and ACLR surgery with intra-op placebo injection
Arm Title
Investigational Arm
Arm Type
Experimental
Arm Description
The investigational arm will receive a pre-op PRP injection, and ACLR surgery with PRP injection
Intervention Type
Procedure
Intervention Name(s)
platelet rich plasma (PRP) injection
Other Intervention Name(s)
Autologous Conditioned Plasma (ACP)
Intervention Description
We aim to evaluate early catabolic and inflammatory changes in knee joints in patients receiving PRP injections following ACL injury, as these patients are at higher risk of developing PTOA. We also aim to establish correlations between markers of biologic activity of PRP and clinical outcomes (including both patient-reported outcomes and clinical functional outcomes), with emphasis on cellular and molecular inflammatory parameters modulated by PRP.
Intervention Type
Procedure
Intervention Name(s)
placebo saline injection
Intervention Description
Patients randomized into the control arm will receive the placebo or saline injection
Primary Outcome Measure Information:
Title
Platelet count (Thousand/uL)
Description
Platelet count (Thousand/uL) will be measured by completing a complete blood count on patient's blood sample.
Time Frame
Baseline
Title
Platelet count (Thousand/uL)
Description
Platelet count (Thousand/uL) will be measured by completing a complete blood count on patient's blood sample.
Time Frame
during the procedure
Title
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
Description
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Time Frame
Baseline
Title
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
Description
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Time Frame
during the procedure
Title
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
Description
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Time Frame
2 weeks post-op
Title
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
Description
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Time Frame
6 weeks post-op
Title
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
Description
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Time Frame
6 months post-op
Title
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
Description
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Time Frame
12 months post-op
Title
Knee Injury and Osteoarthritis Outcome (KOOS-JR)
Description
This survey asks about how the patient feels about their knee. The information helps keep track of how the patient feels about their knee and how well they are able to do their usual activities.
There is no unique measurements. Answer options per question regarding stiffness, pain, function, daily and living are: None, Mild, Moderate, Severe, and Extreme
Time Frame
24 months post-op
Title
Numeric Pain Rating Scale (NPRS)
Description
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
Baseline
Title
Numeric Pain Rating Scale (NPRS)
Description
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
during the procedure
Title
Numeric Pain Rating Scale (NPRS)
Description
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
6 weeks post-op
Title
Numeric Pain Rating Scale (NPRS)
Description
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
6 months post-op
Title
Numeric Pain Rating Scale (NPRS)
Description
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
12 months post-op
Title
Numeric Pain Rating Scale (NPRS)
Description
This survey asks about the patient's pain levels.
Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
24 months post-op
Title
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
Description
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
Baseline
Title
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
Description
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
during the procedure
Title
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
Description
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
2 weeks post-op
Title
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
Description
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
6 weeks post-op
Title
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
Description
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
6 months post-op
Title
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
Description
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
12 months post-op
Title
Patient-Reported Outcomes Measurement Information System 10 (PROMIS-10)
Description
This survey asks about the patient's overall health and quality of life.
Patient will be reporting on a Likert Scale formatted in the following manner for questions 1-6:
5 = "Excellent", 4 = "Very good", 3 = "Good", 2 = "Fair", 1 = "Poor"
Patient will be reporting on a Likert Scale formatted in the following manner for question 7:
5 = "Completely", 4 = "Mostly", 3 = "Moderately", 2 = "A little", 1 = "Not at all"
Patient will be reporting on a Likert Scale formatted in the following manner for question 8:
1= "Never", 2 = "Rarely", 3 = "Sometimes", 4 = "Often", 5 = "Always"
Patient will be reporting on a Likert Scale formatted in the following manner for question 9:
1= "None", 2 = "Mild", 3 = "Moderate", 4 = "Severe", 5 = "Very Severe"
For question 10: Patient will be reporting a score on a scale from 0 to 10, with 0 being "No Pain" and 10 being "Worst Pain Imaginable"
Time Frame
24 months post-op
Title
Single Assessment Numeric Evaluation (SANE)
Description
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Time Frame
Baseline
Title
Single Assessment Numeric Evaluation (SANE)
Description
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Time Frame
during the procedure
Title
Single Assessment Numeric Evaluation (SANE)
Description
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Time Frame
2 weeks post-op
Title
Single Assessment Numeric Evaluation (SANE)
Description
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Time Frame
6 weeks post-op
Title
Single Assessment Numeric Evaluation (SANE)
Description
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Time Frame
6 months post-op
Title
Single Assessment Numeric Evaluation (SANE)
Description
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Time Frame
12 months post-op
Title
Single Assessment Numeric Evaluation (SANE)
Description
This survey asks how the patient feels about their knee.
Patient will be reporting a percentage from 0% to 100%, with 100% being normal.
Time Frame
24 months post-op
Secondary Outcome Measure Information:
Title
Knee stability
Description
Using the KT1000 arthrometer
Time Frame
6 months post-surgery
Title
Knee stability
Description
Using the KT1000 arthrometer
Time Frame
12 months post-surgery
Title
Knee stability
Description
Using the KT1000 arthrometer
Time Frame
24 months post-surgery
Title
Knee strength
Description
Using the Cybex test
Time Frame
6 months post-surgery
Title
Knee strength
Description
Using the Cybex test
Time Frame
12 months post-surgery
Title
Knee strength
Description
Using the Cybex test
Time Frame
24 months post-surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Acute ACL injury within 6 weeks of presentation
Age 14-50
Male or female
Meniscus injury that can be treated with meniscectomy or repair (the lack of meniscus injury will not exclude patients)
Exclusion Criteria:
Prior ACL reconstruction
Prior cartilage repair procedure
Prior meniscus surgery within 12 months
Prior steroid, hyaluronic acid, or PRP injection within 6 months
Other ligament injury requiring repair
Any cartilage lesion requiring repair
Any cartilage lesion greater than grade 2 (partial thickness injury)
History of inflammatory arthritis or joint sepsis
Non English speakers
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jessica Andres-Bergos, PhD
Phone
(917) 260-4694
Email
andresbergosj@hss.edu
Facility Information:
Facility Name
Hospital for Special Surgery
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jessica Andres-Bergos, PhD
Phone
917-260-4694
Email
andresbergosj@hss.edu
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Learn more about this trial
PRP in ACLR to Prevent PTOA
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