ReNu™ Injection to Treat Hip Osteoarthritis Study
Primary Purpose
Osteoarthritis, Hip
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ReNu™ Injection
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis, Hip
Eligibility Criteria
Inclusion Criteria:
- Patients with moderate hip osteoarthritis determined by a combination of clinical and radiographic findings
- Radiographic findings consistent with osteoarthritis as documented by Tonnis radiographic classification (Grade 1 or 2)
- Grade 1 Tonnis changes are defined as mild and include increased sclerosis, slight narrowing of the joint space, no or slight loss of head sphericity
- Grade 2 Tonnis changes are defined as moderate and include small cysts, moderate narrowing of the joint space, moderate loss of head sphericity
- Patients with bilateral grade 1or 2 Tonnis hip osteoarthritis who have bilateral symptoms may have their more symptomatic hip injected. If equivalent symptoms are reported by the patient, then the patient will choose which hip is to be injected. The other Hip can be treated with all standard local interventions that will not have a prolonged systemic effect that could affect the study hip (for example steroid injection, cold therapy, soft braces).
- Between the Ages 18 to 70 with minimum activity level of 2 on the Tegner scale.
- BMI less than 40
- Female patients must be actively practicing a contraception method, abstinence, be surgically sterilized, or be postmenopausal
Exclusion Criteria:
- Pain medication (including NSAIDs) less than 15 days before injection (may take acetaminophen)
- Receiving pain medication other than acetaminophen for conditions unrelated to osteoarthritis of the index hip
- Regular use of anticoagulants, such as Coumadin, dabigatran or rivaroxaban; use of antiplatelet medications are not a reason for exclusion
- History of substance abuse.
- Failure to agree NOT to take additional hip symptom modifying drugs, other than acetaminophen, during the course of the study without reporting to the study team
- Pregnancy or desire to become pregnant during study duration
- Corticosteroid injection into the index hip within 6 months
- Viscosupplement injection into the index hip within 6 months
- Previous open or arthroscopic hip surgery of the involved index hip within the previous 6 months
- Open or arthroscopic surgery of the contralateral hip within the last 6 months
- Worker compensation
- Acute index hip injury (injury within 3 months)
- History of Diabetes mellitus
- History of solid organ or hematologic transplantation
- History of rheumatoid arthritis or other autoimmune disorder
- Diagnosis of a non-basal cell malignancy within the preceding 5 years
- Infection requiring antibiotic treatment within the preceding 3 months
- Current therapy with any immunosuppressive medication, including corticosteroids at a dose > 5 mg per day
Sites / Locations
- Stanford Medicine Orthopaedic Surgery
- Rush University Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
ReNu™ Injection
Arm Description
ReNu™ is an allograft tissue composed of particularized amniotic membrane and cell from the amniotic fluid.
Outcomes
Primary Outcome Measures
IHOT12 - International Hip Outcome Tool 12
Change from Baseline
Visual Analog Scale (VAS) Pain Scale
Change from Baseline
Secondary Outcome Measures
Modified Harris Hip Score
Change from Baseline
SF12 Score
Generic measure of patient's health status change from baseline
Single Assessment Numerical Evaluation (SANE)
Measurement tool used to record patient's self-reported change in function from baseline
Full Information
NCT ID
NCT03063099
First Posted
February 21, 2017
Last Updated
January 13, 2020
Sponsor
NuTech Medical, Inc
Collaborators
Organogenesis
1. Study Identification
Unique Protocol Identification Number
NCT03063099
Brief Title
ReNu™ Injection to Treat Hip Osteoarthritis Study
Official Title
A Pilot Study of ReNu™ Hip Injection: Monitoring the Response of Hip Function and Pain in Patient With Osteoarthritis
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
February 8, 2017 (Actual)
Primary Completion Date
June 28, 2019 (Actual)
Study Completion Date
June 28, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NuTech Medical, Inc
Collaborators
Organogenesis
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A pilot study to evaluate changes in hip function and pain in patients with osteoarthritis receiving the ReNu™ Hip Injection.
Detailed Description
This is a prospective, non-randomized pilot study evaluating the efficacy of ReNu™ hip injection on patients with moderate osteoarthritis. The effects will be measured primarily through patient-reported outcomes questionnaires after a single injection. Patients will be followed up to 12 months to evaluate improvements using common pain and function subscales.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Hip
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ReNu™ Injection
Arm Type
Experimental
Arm Description
ReNu™ is an allograft tissue composed of particularized amniotic membrane and cell from the amniotic fluid.
Intervention Type
Other
Intervention Name(s)
ReNu™ Injection
Intervention Description
Injection into the hip for the treatment of Osteoarthritis.
Primary Outcome Measure Information:
Title
IHOT12 - International Hip Outcome Tool 12
Description
Change from Baseline
Time Frame
3 & 6 months
Title
Visual Analog Scale (VAS) Pain Scale
Description
Change from Baseline
Time Frame
3 & 6 months
Secondary Outcome Measure Information:
Title
Modified Harris Hip Score
Description
Change from Baseline
Time Frame
3, 6 & 12 months
Title
SF12 Score
Description
Generic measure of patient's health status change from baseline
Time Frame
3, 6 & 12 months
Title
Single Assessment Numerical Evaluation (SANE)
Description
Measurement tool used to record patient's self-reported change in function from baseline
Time Frame
3, 6 & 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with moderate hip osteoarthritis determined by a combination of clinical and radiographic findings
Radiographic findings consistent with osteoarthritis as documented by Tonnis radiographic classification (Grade 1 or 2)
Grade 1 Tonnis changes are defined as mild and include increased sclerosis, slight narrowing of the joint space, no or slight loss of head sphericity
Grade 2 Tonnis changes are defined as moderate and include small cysts, moderate narrowing of the joint space, moderate loss of head sphericity
Patients with bilateral grade 1or 2 Tonnis hip osteoarthritis who have bilateral symptoms may have their more symptomatic hip injected. If equivalent symptoms are reported by the patient, then the patient will choose which hip is to be injected. The other Hip can be treated with all standard local interventions that will not have a prolonged systemic effect that could affect the study hip (for example steroid injection, cold therapy, soft braces).
Between the Ages 18 to 70 with minimum activity level of 2 on the Tegner scale.
BMI less than 40
Female patients must be actively practicing a contraception method, abstinence, be surgically sterilized, or be postmenopausal
Exclusion Criteria:
Pain medication (including NSAIDs) less than 15 days before injection (may take acetaminophen)
Receiving pain medication other than acetaminophen for conditions unrelated to osteoarthritis of the index hip
Regular use of anticoagulants, such as Coumadin, dabigatran or rivaroxaban; use of antiplatelet medications are not a reason for exclusion
History of substance abuse.
Failure to agree NOT to take additional hip symptom modifying drugs, other than acetaminophen, during the course of the study without reporting to the study team
Pregnancy or desire to become pregnant during study duration
Corticosteroid injection into the index hip within 6 months
Viscosupplement injection into the index hip within 6 months
Previous open or arthroscopic hip surgery of the involved index hip within the previous 6 months
Open or arthroscopic surgery of the contralateral hip within the last 6 months
Worker compensation
Acute index hip injury (injury within 3 months)
History of Diabetes mellitus
History of solid organ or hematologic transplantation
History of rheumatoid arthritis or other autoimmune disorder
Diagnosis of a non-basal cell malignancy within the preceding 5 years
Infection requiring antibiotic treatment within the preceding 3 months
Current therapy with any immunosuppressive medication, including corticosteroids at a dose > 5 mg per day
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katie Mowry, PhD
Organizational Affiliation
Organogenesis
Official's Role
Study Director
Facility Information:
Facility Name
Stanford Medicine Orthopaedic Surgery
City
Redwood City
State/Province
California
ZIP/Postal Code
94063
Country
United States
Facility Name
Rush University Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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ReNu™ Injection to Treat Hip Osteoarthritis Study
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