Treatment of Partial-Thickness Rotator Cuff Tears
Public ClinicalTrials.gov record NCT03734536. 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
Prospective Multi-center Study Comparing REGENETEN in Lieu of Standard Arthroscopic Repair of High-grade (>50%) Partial-thickness Tears
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The goal of this clinical trial is to demonstrate that REGENETEN is superior to standard repair techniques when surgically treating high-grade (\>50%) partial-thickness tears.
Study identification
- NCT ID
- NCT03734536
- Recruitment status
- Terminated
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 168 participants
Conditions and interventions
Interventions
- REGENETEN™ Bioinductive Implant Device
- Arthroscopic repair of the high-grade (>50%) partial-thickness Device
Device
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Dec 4, 2018
- Primary completion
- Sep 10, 2023
- Completion
- Sep 10, 2023
- Last update posted
- Nov 18, 2024
2018 – 2023
United States locations
- U.S. sites
- 10
- U.S. states
- 8
- U.S. cities
- 10
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of Florida Orthopaedics and Sports Medicine | Gainesville | Florida | 32607 | — |
| Baptist Health | Jacksonville Beach | Florida | 32250 | — |
| Harbin Clinic | Rome | Georgia | 30165 | — |
| University of Kentucky | Lexington | Kentucky | 40506 | — |
| Ochsner Health Center | New Orleans | Louisiana | 70121 | — |
| Anne Arundel Medical Center/Luminis Health | Annapolis | Maryland | 21401 | — |
| Syracuse Orthopedic Specialist | DeWitt | New York | 13214 | — |
| Columbia University | New York | New York | 10032 | — |
| Orthopedic Associates of SW Ohio | Centerville | Ohio | 45459 | — |
| Texas Orthopedic Specialists | Bedford | Texas | 76021 | — |
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 NCT03734536, 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 Nov 18, 2024 · Synced Sep 5, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT03734536 live on ClinicalTrials.gov.