Autologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears
Public ClinicalTrials.gov record NCT03752827. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Prospective, Double-Blinded, Multi-Center Pivotal Trial of Autologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this investigation is to evaluate the safety and superior effectiveness in functional improvement in patients with partial-thickness rotator cuff tears (PTRCTs) after the administration of a single injection of adipose-derived regenerative cells (ADRCs) into the partial-thickness rotator cuff tear compared to the administration of a single corticosteroid injection into the associated subacromial space.
Study identification
- NCT ID
- NCT03752827
- Recruitment status
- Active, not recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 168 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 30 Years to 75 Years
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- May 12, 2019
- Primary completion
- Nov 29, 2023
- Completion
- Nov 30, 2025
- Last update posted
- Aug 19, 2025
2019 – 2025
United States locations
- U.S. sites
- 14
- U.S. states
- 9
- U.S. cities
- 14
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Arizona Research Center | Phoenix | Arizona | 85053 | — |
| Biosolutions Clinical Research Center | La Mesa | California | 91942 | — |
| Lotus Clinical Research, LLC | Pasadena | California | 91105 | — |
| Sports and Orthopedic Center | Coral Springs | Florida | 33067 | — |
| Universal Axon Clinical Research | Doral | Florida | 33166 | — |
| Shrock Clinical Research | Fort Lauderdale | Florida | 33316 | — |
| Andrews Institute for Orthopaedics and Sports Medicine | Gulf Breeze | Florida | 32561 | — |
| Georgia Institute for Clinical Research | Marietta | Georgia | 30060 | — |
| Tulane University School of Medicine | New Orleans | Louisiana | 70112 | — |
| University of Michigan | Ann Arbor | Michigan | 48105 | — |
| Sanford Medical Center | Fargo | North Dakota | 58103 | — |
| Sanford Orthopedic Clinic/Research | Sioux Falls | South Dakota | 57104 | — |
| HD Research | Houston | Texas | 77041 | — |
| Texas Plastic Surgery | San Antonio | Texas | 78240 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT03752827, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 19, 2025 · Synced Sep 6, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT03752827 live on ClinicalTrials.gov.