Intra-articular Adipose Tissue Injections for Osteoarthritis
Primary Purpose
Osteoarthritis, Knee
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Autologous adipose tissue injection
Hyaluronic Acid
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis, Knee
Eligibility Criteria
Inclusion Criteria:
- Age 45 to 75, inclusive
- Normal axial alignment
- X-ray, Kellgren-Lawrence OA grade 2 - 3, inclusive
- WOMAC-pain: Between 9 and 19, inclusive
- Willingness to participate all scheduled follow-ups
- Willingness to refrain from taking NSAIDs, level 2 analgesics, and opioids for the course of the study
- BMI < 40
Exclusion Criteria:
- Pregnant or lactating
- Intra-articular injection within 3 months of treatment
- Inflammatory arthritis
- Any disease or active drug use that significantly compromises coagulation
- Significant damage and/or tears of the ACL or other supporting tissues
- Prior knee surgery in the last 6 months in the knee that will be injected
- Active tobacco use
- Active alcohol or substance abuse within 6 months of study entry
- Known hypersensitivity (allergy) to hyaluronan (sodium hyaluronate) preparations
- Knee joint infections, skin diseases or infections in the area of the injection site
- Diabetes
- Active inhaler use
- Any medical condition, which in the opinion of the clinical investigator, would interfere with the treatment or outcome evaluation
Sites / Locations
- Keck Medicine of USCRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Autologous adipose tissue knee injection
Hyaluronic Acid knee injection
Arm Description
Fat will be removed from the abdomen and processed using the Lipogems device. Approximately 5ml of the microfragmented fat product will be injected into the knee joint.
Hyaluronic Acid - Synvisc-One®: A high molecular weight sodium hyaluronate (HA). HA is an FDA approved, standard of care treatment.
Outcomes
Primary Outcome Measures
The pain items of then Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC-A)
WOMAC-A is a widely used, proprietary set of standardized questionnaires used by health professionals to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain.
Secondary Outcome Measures
Patient-Reported Outcomes Measurement Information System 29-item (PROMIS®-29)
A collection of 4-item short forms assessing anxiety, depression, fatigue, pain interference, physical function, sleep disturbance, and ability to participate in social roles and activities as well as a single pain intensity item.
Western Ontario and McMaster Universities Osteoarthritis Index
WOMAC is a widely used, proprietary set of standardized questionnaires used by health professionals to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain, stiffness, and physical functioning of the joints.
Clinical Anchors
Clinical anchors will be used to identify minimal important differences in treatment groups
Full Information
NCT ID
NCT03242707
First Posted
July 28, 2017
Last Updated
October 2, 2019
Sponsor
University of Southern California
1. Study Identification
Unique Protocol Identification Number
NCT03242707
Brief Title
Intra-articular Adipose Tissue Injections for Osteoarthritis
Official Title
A Randomized, Controlled Study to Evaluate the Efficacy of Intra-articular, Autologous Adipose Tissue Injections for the Treatment of Mild-to-Moderate Osteoarthritis
Study Type
Interventional
2. Study Status
Record Verification Date
October 2019
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
December 1, 2019 (Anticipated)
Study Completion Date
December 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A new generation of "minimally manipulated" regenerative treatments are being offered at clinics across the country, but there is no strong efficacy data to support their use. The purpose of this study is to estimate the effect size of the treatment by comparing the efficacy of autologous fat to the current standard of care treatment, hyaluronic acid (HA). As a secondary aim, we will test for preliminary evidence of efficacy of autologous fat vs. HA and determine how these treatments effect the biochemical environment of the knee by comparing pre-injection and post-injection synovial fluid biomarker profiles.
Detailed Description
In recent years, fat treatments administered for structural reconstruction, repair, or replacement are being increasingly offered at clinics across the country. These treatments contain both autologous cells that are often referred to as "stem cells" or "MSCs" and extra-cellular matrix (ECM). Cell therapies containing ECM are thought to have the following advantages over treatments prepared using enzymatic digestion: (1) preservation of the stromal vascular niche, which allows time-release of the regenerative factors; (2) release of bioactive molecules by exosomes, which have been demonstrated to be significantly greater in mechanically processed fat than enzymatically processed fat; and (3) maintenance of the structural and morphologic unit, which is thought to increase cell efficacy by making the cells more resilient to the harsh conditions in the recipient environment. Case reports investigating the use of autologous fat treatments show promise, but a number of questions remain unanswered. Agents injected into the joint tend to be quickly cleared from the body and ECM itself has the potential to produce inflammatory signals and induce osteoarthritis.
This study will use a Hyaluronic acid (HA) as an active control, which is the standard of care for pain associated with osteoarthritis. The use of HA as an active control for autologous cell-based therapies is well established and is the best option given the need to aspirate fat tissue from patients who will be receiving the study treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly assigned to receive either a single autologous fat injection or a single hyaluronic acid injection.
Masking
None (Open Label)
Masking Description
Patients will know which group they have been assigned to
Allocation
Randomized
Enrollment
54 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Autologous adipose tissue knee injection
Arm Type
Experimental
Arm Description
Fat will be removed from the abdomen and processed using the Lipogems device. Approximately 5ml of the microfragmented fat product will be injected into the knee joint.
Arm Title
Hyaluronic Acid knee injection
Arm Type
Active Comparator
Arm Description
Hyaluronic Acid - Synvisc-One®: A high molecular weight sodium hyaluronate (HA). HA is an FDA approved, standard of care treatment.
Intervention Type
Biological
Intervention Name(s)
Autologous adipose tissue injection
Other Intervention Name(s)
Lipogems, Microfragmented fat
Intervention Description
20ml to 40ml of subcutaneous adipose tissue will be aspirated from the abdomen. Adipose tissue will be processed using the Lipogems device, a closed-loop processing device used in medical procedures involving the harvesting, concentrating and transferring of autologous adipose tissue.
The resulting fat product will be delivered locally via ultrasound-guided, intra-articular injection.
Intervention Type
Drug
Intervention Name(s)
Hyaluronic Acid
Intervention Description
Synvisc-One® is a high molecular weight sodium hyaluronate.
Primary Outcome Measure Information:
Title
The pain items of then Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC-A)
Description
WOMAC-A is a widely used, proprietary set of standardized questionnaires used by health professionals to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain.
Time Frame
Change from baseline WOMAC score at 6 months
Secondary Outcome Measure Information:
Title
Patient-Reported Outcomes Measurement Information System 29-item (PROMIS®-29)
Description
A collection of 4-item short forms assessing anxiety, depression, fatigue, pain interference, physical function, sleep disturbance, and ability to participate in social roles and activities as well as a single pain intensity item.
Time Frame
Change from baseline in PROMIS-29 from baseline to 6 months
Title
Western Ontario and McMaster Universities Osteoarthritis Index
Description
WOMAC is a widely used, proprietary set of standardized questionnaires used by health professionals to evaluate the condition of patients with osteoarthritis of the knee and hip, including pain, stiffness, and physical functioning of the joints.
Time Frame
Change from baseline in PROMIS-29 from baseline to 6 months
Title
Clinical Anchors
Description
Clinical anchors will be used to identify minimal important differences in treatment groups
Time Frame
Clinical anchors from baseline to 6 months
Other Pre-specified Outcome Measures:
Title
Synovial fluid analysis
Description
Selected OA biomarker profiles that define different OA phenotypes predict the responses to autologous adipose tissue injections
Time Frame
Baseline, 6 weeks and 6 months
Title
Short-term clinical evaluation - WOMAC
Description
WOMAC questionnaire will be administered at the 6-week follow-up
Time Frame
Change from baseline at 6 weeks
Title
Short-term clinical evaluation - PROMIS
Description
PROMIS questionnaire will be administered at the 6-week follow-up
Time Frame
Change from baseline at 6 weeks
Title
Force Plate Analysis
Description
Balance will be assessed using a proprietary force plate system at baseline, 6 weeks and 6 months.
Time Frame
Assessment and change from baseline to 6 weeks and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 45 to 75, inclusive
Normal axial alignment
X-ray, Kellgren-Lawrence OA grade 2 - 3, inclusive
WOMAC-pain: Between 9 and 19, inclusive
Willingness to participate all scheduled follow-ups
Willingness to refrain from taking NSAIDs, level 2 analgesics, and opioids for the course of the study
BMI < 40
Exclusion Criteria:
Pregnant or lactating
Intra-articular injection within 3 months of treatment
Inflammatory arthritis
Any disease or active drug use that significantly compromises coagulation
Significant damage and/or tears of the ACL or other supporting tissues
Prior knee surgery in the last 6 months in the knee that will be injected
Active tobacco use
Active alcohol or substance abuse within 6 months of study entry
Known hypersensitivity (allergy) to hyaluronan (sodium hyaluronate) preparations
Knee joint infections, skin diseases or infections in the area of the injection site
Diabetes
Active inhaler use
Any medical condition, which in the opinion of the clinical investigator, would interfere with the treatment or outcome evaluation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
William Fang
Phone
323-442-6959
Email
williahf@usc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
C.Thomas Vangsness, MD
Organizational Affiliation
Keck School of Medicine of USC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Keck Medicine of USC
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
William Fang
Phone
323-442-6959
Email
williahf@usc.edu
12. IPD Sharing Statement
Citations:
PubMed Identifier
30355323
Citation
Jones IA, Wilson M, Togashi R, Han B, Mircheff AK, Thomas Vangsness C Jr. A randomized, controlled study to evaluate the efficacy of intra-articular, autologous adipose tissue injections for the treatment of mild-to-moderate knee osteoarthritis compared to hyaluronic acid: a study protocol. BMC Musculoskelet Disord. 2018 Oct 24;19(1):383. doi: 10.1186/s12891-018-2300-7.
Results Reference
derived
Learn more about this trial
Intra-articular Adipose Tissue Injections for Osteoarthritis
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