search
Back to results

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
NuTech Medical, Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Hip

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
February 21, 2017
Last Updated
January 13, 2020
Sponsor
NuTech Medical, Inc
Collaborators
Organogenesis
search

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

Learn more about this trial

ReNu™ Injection to Treat Hip Osteoarthritis Study

We'll reach out to this number within 24 hrs