Clinical trials: Full Rotator Cuff Tear, open to volunteers
Rotator Cuff Tears, Rotator Cuff Tear Arthropathy
Bioinductive Patch for Full-Thickness Rotator Cuff Tears
The purpose of this randomized-controlled study is to compare outcomes of arthroscopic rotator cuff repair augmented with a Bioinductive Implant (study group) to standard arthroscopic rotator cuff repair (control group).
- Trial name
- NCT05439850
- Testing
- arthroscopic rotator cuff repair, Bioinductive implant, Ultrasound Imaging
- Where
- United States
- Volunteers
- 78 people
- Sponsor
- Henry Ford Health System
Partial Rotator Cuff Tears, Rotator Cuff Injuries
Concentric vs Eccentric Full Can Exercise in Partial Rotator Cuff Tears
This study aims to compare the effects of concentric and eccentric full can exercises on supraspinatus muscle architecture in individuals with partial rotator cuff tears.
- Conditions
- Partial Rotator Cuff Tears, Rotator Cuff Injuries, Shoulder Pain Syndrome
- Trial name
- FULLCAN-PRCT (NCT07587931)
- Testing
- Concentric Full Can Exercise, Eccentric Full Can Exercise, Standard Physiotherapy Program
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Firat University
Full Rotator Cuff Tear, Microfracture Procedure
Does Medial Raw Anchor Necessary During Tendon Repair Combined With Microfracture
This study is a prospective randomized controlled study of rotator cuff repair with lateral raw or double raw combined with microfracture procedure.
- Conditions
- Full Rotator Cuff Tear, Microfracture Procedure, Double Raw Repair, Lateral Raw Repair
- Trial name
- NCT06431191
- Testing
- lateral raw, double raw
- Where
- China
- Volunteers
- 50 people
- Sponsor
- Beijing Jishuitan Hospital
High-grade Partial or Full Thickness Rotator Cuff Tears
Cold and Compression After Rotator Cuff Repair (RCR)
The purpose of this study is to compare pain score (Patient-Reported Outcomes Measurement Information System: PROMIS NRS Pain Subscale) between the control and cold/compression groups pre-surgically, daily after surgery for 14…
- Trial name
- NCT07516327
- Testing
- SOC (Standard of care), Cold and Compression
- Where
- United States
- Volunteers
- 90 people
- Sponsor
- Ochsner Health System
SLAP Lesion
Biceps Tenodesis With 360 Suture Anchor Versus Self Locking Tenodesis In the Absence of Rotator Cuff Tears
This is a prospective randomized controlled trial. The aim of this study is to compare the clinical results and complications of self-locking biceps tenodesis and double-loop 360 lasso biceps tenodesis for the treatment of…
- Trial name
- Blast2 (NCT06772103)
- Testing
- self-locking biceps tenodesis, Biceps Tenodesis with 360 Suture anchor
- Where
- France
- Volunteers
- 98 people
- Sponsor
- Clinique Générale dAnnecy
Rotator Cuff Tears
InSpace Accelerated Rehabilitation Study
This is a prospective, parallel group, open-label, multi- center, randomized study to assess two accelerated rehabilitation programs for use with the InSpace device in the treatment of full thickness Massive, Irreparable Rotator…
- Trial name
- iAccelerate (NCT05329584)
- Testing
- InSpace Subacromial Tissue Spacer
- Where
- 11 sites in United States
- Volunteers
- 160 people, healthy volunteers welcome
- Sponsor
- Stryker Endoscopy
Rotator Cuff Injuries
Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant
This prospective, single-arm, multicenter registry is being conducted to collect real world post-market data from patients who are undergoing rotator cuff repair using the REGENETEN◊ Bioinductive Implant System.
- Trial name
- RePaRe (NCT06857084)
- Testing
- Arthroscopic rotator cuff repair with REGENETEN Bioinductive Implant augmentation
- Where
- 22 sites in Australia, Germany and 2 more
- Volunteers
- 400 people
- Sponsor
- Smith & Nephew, Inc.