A Disease-based Treatment Study for Diagnosed Osteoarthritis Utilizing Adipose-derived Regenerative Cells

NCT ID: NCT04405297

Last Updated: 2025-10-22

Basic Information

• Recruitment Status: TERMINATED
• Total Enrollment: 14 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-05-24
• Study Completion Date: 2024-09-23

Brief Summary

This is a prospective, multi-location safety and effectiveness study, and data registry of autologous adult ADRCs generated by the Transpose® RT System in subjects with OA in the shoulder, wrist, knee, hip, or ankle.

Detailed Description

Subjects who have signed informed consent and Health Insurance Portability and Accountability Act (HIPPA) authorization, and are determined to meet all inclusion criteria and no exclusion criteria will be enrolled in this study and receive the ADRC treatment.

The subject will have an injection procedure (ADRC treatment) For this study, a licensed physician trained in liposuction must perform the syringe liposuction procedure. The licensed physician who performs the lipoplasty may be the Investigator or a non-Investigator physician (e.g., a plastic surgeon) who is trained on the study protocol.

All subjects will undergo a minor syringe liposuction procedure to acquire approximately 100 mL of lipoaspirate for preparation of ADRC using the Transpose® RT System. The removed tissue is processed to extract a cell suspension (the cell product). Once the cell product has been obtained, tested, and found to conform to release criteria, the subject will be treated with the ADRCs.

Conditions

Knee Osteoarthritis; Hip Osteoarthritis; Ankle Osteoarthritis; Shoulder Osteoarthritis; Wrist Osteoarthritis

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Hip Osteoarthritis

Subjects will receive autologous adipose-derived regenerative stem cells into their affected hip joint.

Adipose-derived regenerative cells

Intervention Type: DEVICE

Adipose-derived regenerative cells will be obtained from a small-volume lipoaspirate procedure. The lipoaspirate will then be enzymatically digested to produce a stromal vascular fraction (SVF) that will be injected into the targeted joint.

Knee Osteoarthritis

Subjects will receive autologous adipose-derived regenerative stem cells into their affected knee joint.

Adipose-derived regenerative cells

Intervention Type: DEVICE

Adipose-derived regenerative cells will be obtained from a small-volume lipoaspirate procedure. The lipoaspirate will then be enzymatically digested to produce a stromal vascular fraction (SVF) that will be injected into the targeted joint.

Ankle Osteoarthritis

Subjects will receive autologous adipose-derived regenerative stem cells into their affected ankle joint.

Adipose-derived regenerative cells

Intervention Type: DEVICE

Adipose-derived regenerative cells will be obtained from a small-volume lipoaspirate procedure. The lipoaspirate will then be enzymatically digested to produce a stromal vascular fraction (SVF) that will be injected into the targeted joint.

Shoulder Osteoarthritis

Subjects will receive autologous adipose-derived regenerative stem cells into their affected shoulder joint.

Adipose-derived regenerative cells

Intervention Type: DEVICE

Adipose-derived regenerative cells will be obtained from a small-volume lipoaspirate procedure. The lipoaspirate will then be enzymatically digested to produce a stromal vascular fraction (SVF) that will be injected into the targeted joint.

Wrist Osteoarthritis

Subjects will receive autologous adipose-derived regenerative stem cells into their affected wrist joint.

Adipose-derived regenerative cells

Intervention Type: DEVICE

Adipose-derived regenerative cells will be obtained from a small-volume lipoaspirate procedure. The lipoaspirate will then be enzymatically digested to produce a stromal vascular fraction (SVF) that will be injected into the targeted joint.

Interventions

Adipose-derived regenerative cells

Adipose-derived regenerative cells will be obtained from a small-volume lipoaspirate procedure. The lipoaspirate will then be enzymatically digested to produce a stromal vascular fraction (SVF) that will be injected into the targeted joint.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Men and women age 18 or older

2. Clinical and radiographic diagnosis of OA in one of the following areas: Ankle, Hip, Knee, Shoulder, or Wrist

3. Continued OA pain in the targeted joint despite conservative measures (per treating provider's discretion)

4. Average daily VAS Pain Score ≥3

5. Understand and provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization prior to initiation of any study-specific procedures

6. On physical exam. subject appears to have adequate adipose tissue for liposuction

Ankle Cohort:

1. Currently Kellgren-Lawrence Grade II, III or IV in the ankle based on X-ray (weight-bearing mortise views with 20⁰ internal rotation)

2. Ankle pain for at least 6 months, despite conservative treatment or inability to tolerate the side effects of medications

3. Normal activity level, not bedridden or confined to a wheelchair, able to walk 30 meters without the aid of a walker, crutches or cane

Hip Cohort:

1. Hip OA diagnosed on x-ray and/or Magnetic Resonance Imaging (MRI) (Tӧnnis grade 1, 2, or 3)

Knee Cohort:

1. Kellgren-Lawrence system of Grade II, III, or IV

2. Subject may have concomitant patellofemoral but they must have stage II or higher generalized knee OA

Shoulder Cohort:

1. Grades 1, 2 or 3 OA in the index glenohumeral joint based on the Samilson-Prieto classification system as confirmed by X-ray (axillary view and true anterior-posterior view)

2. Subjects who have failed standard non-surgical management of their shoulder arthritis who would benefit from a shoulder arthroplasty. Failed medical management will be defined as persistent pain and disability despite adequate standard non-operative management for 6 months. Medical management will be defined as:

1. The use of drugs including analgesics and non-steroidal anti-inflammatory drugs

2. Activity modification

Wrist Cohort:

1. Clinical symptoms consistent with wrist OA

Exclusion Criteria

2. Viscosupplementation within 6 months of screening in the targeted joint

3. Other Biologic Injection (Platelet Rich Plasma (PRP) or stem cell) within 6 months in the targeted joint

4. Surgery in the targeted joint within the past 6 months (either open or scope)

5. Planned/anticipated surgery of the targeted joint during study participation

6. Systemic or intra-articular injection of corticosteroids in any joint within 3 months before screening (re-screening allowed once this criteria is met)

7. Females of childbearing age who have not used or do not plan to use acceptable birth control measures, for the duration of the study. Oral, injected or implanted hormonal contraceptive, barrier methods (condom or diaphragm with spermicide), intrauterine device, surgical sterilization, transdermal delivery, congenital sterility or sexual abstinence are considered acceptable forms of birth control. If sexually active, the subject must have been using one of the accepted birth control methods at least one month prior to study entry.

8. Part of a vulnerable population per Office for Human Research Protections (OHRP) definition (pregnant women and breast-feeding women, cognitively impaired, prisoners, etc.)

9. Unwilling to discontinue the use of Non-Steroidal Anti-Inflammatory (NSAID)s for 7 calendar days prior to the procedure

10. Unwilling to discontinue NSAIDS for 5 calendar days after procedure

11. Insufficient amount of subcutaneous tissue to allow recovery of at least 100mL of lipoaspirate

12. Diagnosed musculoskeletal cancer or any diagnosed cancer, other than musculoskeletal if not on long term remission (e.g. at least 5 years or negative biopsy at last exam), except basal cell carcinoma

13. Have received chronic (more than 7 consecutive days) treatment with systemic corticosteroids at a dose equivalent to prednisone ≥ 10 mg/day within 14 days prior to an injection procedure.

14. Subject is currently participating in another clinical trial that has not yet completed its primary endpoint. (Nonintervention observational studies are not exclusionary.)

15. History of, or ongoing, autoimmune disorder that requires treatment with an immunosuppressive medication

16. Subjects who have a documented history or presence of inflammatory arthritis, rheumatoid arthritis, and sepsis in the treatment site

17. History of bleeding disorders or inflammatory joint disease

18. Inability to hold anti-platelet therapy according to treating provider prior to procedure

19. Any medical condition that could preclude participation in the study in the opinion of the investigator

20. Active workers' compensation case in progress with the targeted joint

21. Daily opioid use for the 3 months prior to screening or anticipated daily use while participating on study

22. Psychiatric disorder that may prevent participation in the study in the opinion of the investigators

23. A positive screen for human immunodeficiency virus (HIV) by antibodies or nucleic acid test

24. Has a known active Hepatitis B (e.g. HBsAg reactive) or Hepatitis C (e.g. HCV RNA [qualitative] is detected)

25. Allergy to sodium citrate of any "caine" type of local anesthetic

26. Hemoglobin less than 10g/dL at the time of screening

27. Leukocytes <3,000/µL; neutrophils <1,500/µL; lymphocytes <800/µL; platelets <100,000/µL at the time of screening

28. Subjects with a known diagnosis of osteoporosis

29. Diagnosis of liver disease as defined by alanine aminotransferase (ALT) >2x the upper limit of age-determined normal (ULN) or total bilirubin > 1.5x ULN

Ankle Cohort:

1. Lower leg trauma in a location other than within the ankle

2. Arthroscopy or open surgery of the ankle joint within 6 months of screening.

3. Extreme obesity, as defined by National Institutes of Health (NIH) Clinical Guidelines Body Mass Index (BMI > 40)

4. Any condition other than OA of the ankle joint which, in the opinion of the investigator, affects their ability to ambulate to a sufficient degree to interfere with the assessment of the safety and treatment effects of the study injection.

Hip Cohort:

1. Evidence of hip dysplasia (centre edge angle less than 20⁰)

2. Previous fracture trauma to the affected hip requiring medical or surgical treatment

3. Severe acetabular deformities (e.g. acetabular protrusion, coxa profunda, circumferential labral ossification)

4. Infections or skin diseases at target hip joint

5. Significant medical co-morbidities (requiring daily assistance for activities of daily living)

6. Any clinically significant or symptomatic vascular or neurologic disorder of the lower extremities

7. Extreme obesity, as defined by NIH Clinical Guidelines Body Mass Index (BMI>40)

8. Femoral head deformity (perthes or AVN)

Knee Cohort:

1. Extreme obesity, as defined by NIH Clinical Guidelines Body Mass Index (BMI>40)

2. Clinically apparent tense effusion of the targeted knee

3. Significant valgus/varus deformities (+/- 10⁰)

Shoulder Cohort:

1. Walch B2 glenoid with greater than 10⁰ of retroversion

2. Active joint or systemic infection

3. Rotator cuff arthropathy

4. Significant muscle paralysis

5. Charcot's arthropathy

Wrist Cohort:

1. Subjects who have a documented diagnosis of active carpal tunnel syndrome

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sanford Health

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David A. Pearce, PhD

Role: PRINCIPAL_INVESTIGATOR

Sanford Health

Locations

Sanford Orthopedics and Sports Medicine

Sioux Falls, South Dakota, United States

Countries

United States

Other Identifiers

ENDURE

Identifier Type: -

Identifier Source: org_study_id