Clinical trials: Rotator Cuff Repairs, open to volunteers
Rotator Cuff Syndrome
Study Comparing Two Anesthetics for Arthroscopic Rotator Cuff Repair
The purpose of this study is to to compare the post-anesthetic recovery time to awake consciousness and hemodynamic and ventilatory capacities for discharge from the Post-Interventional Monitoring Room in patients admitted for…
- Trial name
- ALRAGA (NCT07093905)
- Testing
- arthroscopy of the shoulder rotator cuff
- Where
- France
- Volunteers
- 34 people
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche
Rotator Cuff Injury, Rotator Cuff Tear
Blood Flow Restriction Exercise-induced Hypoalgesia
The goal of this crossover randomized clinical trial is to compare the acute effect on exercise-induced hypoalgesia (EIH) between isometric exercise with blood flow restriction (BFR) and isometric exercise alone in adults…
- Conditions
- Rotator Cuff Injury, Rotator Cuff Tear, Rotator Cuff Repair
- Trial name
- NCT06924112
- Testing
- Isometric exercises, Isometric exercises with BFR
- Where
- Chile
- Volunteers
- 22 people
- Sponsor
- University of Valencia
Shoulder Arthroscopy, Interscalene Nerve Block
Effect of Anesthesia Technique on Surgical View in Shoulder Arthroscopy
This prospective observational study evaluates the effect of the anesthesia method (general anesthesia versus regional anesthesia [interscalene nerve block/superficial cervical block] with sedation) on the operating clarity of…
- Conditions
- Shoulder Arthroscopy, Interscalene Nerve Block, Surgical View Quality, Surgeon Satisfaction
- Trial name
- NCT07343414
- Where
- Turkey (Türkiye)
- Volunteers
- 82 people
- Sponsor
- Amasya University
Shoulder Injuries, Rotator Cuff Injuries
Subscap Reverse Shoulder Arthroplasty
The subscapularis is part of the rotator cuff and is release as part of a reverse shoulder replacement. The decision to repair this tendon is controversial.
- Trial name
- NCT05344898
- Testing
- Subscap Tenotomy, Subscap Repair
- Where
- United States
- Volunteers
- 118 people, healthy volunteers welcome
- Sponsor
- University of Maryland, Baltimore
Early Retears and Clinical Outcomes Following Surgical Repair of Massive Rotator Cuff Tears
Postoperative USG Control and Clinical Follow-up of Massive Rotator Cuff Tendon Ruptures
This prospective observational study aims to investigate the tendon integrity and clinical outcomes following surgical repair of massive rotator cuff tears.
- Trial name
- NCT07004218
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Gazi University
Rotator Cuff
Arthroscopic Treatment of Rotator Cuff Tears
Rotator cuff tears are the primary cause of shoulder pain and functional impairment, accounting for 50% to 85% of shoulder disorders.
- Trial name
- NCT06961318
- Where
- China
- Volunteers
- 600 people
- Sponsor
- Peking University Third Hospital
Rotator Cuff Tears
Rotator Cuff Tears Repair With or Without Dermal Patch Augmentation
The Investigators are planning to conduct a Pilot study of 40 patients of Pragmatic randomised controlled trial comparing rotator cuff tendons repair (small tendons around the shoulder ) with or without augmentative patch.
- Trial name
- CUFFPATCH (NCT04975581)
- Testing
- Allograft Patch
- Where
- United Kingdom
- Volunteers
- 40 people
- Sponsor
- University Hospitals, Leicester
Rotator Cuff Tears, Rotator Cuff Injuries
Arthroscopic Rotator Cuff Repair With Long Head of Biceps Transposition and Acellular Dermal Matrix Augmentation for Large to Massive Incompletely Repairable Rotator Cuff Tears
Large-to-massive rotator cuff tears of the shoulder with poor tendon and muscle quality often cannot be fully repaired back to its footprint, and they have a high risk of re-tear.
- Conditions
- Rotator Cuff Tears, Rotator Cuff Injuries, Massive Rotator Cuff Tear
- Trial name
- SCR-ADM-repair (NCT07875556)
- Testing
- Rotator Cuff Repair, Long Head of the Biceps Tendon Transposition, Acellular Dermal Matrix (Allograft) Augmentation
- Where
- Vietnam
- Volunteers
- 40 people
- Sponsor
- Tam Anh Research Institute
Rotator Cuff Tear Surgical Repair
H-Wave® Device Stimulation for Post-operative Rotator Cuff Repair Surgery
The goal of this intent-to-treat study is to evaluate the efficacy of H-Wave Device Stimulation following rotator cuff repair surgery.
- Trial name
- NCT07501949
- Testing
- Routine post-surgical care plus H-Wave® Device Stimulation (HWDS), Routine post-surgical care
- Where
- 4 sites in United States
- Volunteers
- 80 people
- Sponsor
- Electronic Waveform Lab
Supraspinatus Tear
A Study on the Effectiveness of Preventive Extensive Release of the Rotator Interval and Joint Capsule to Reduce Postoperative Stiffness in Arthroscopic Rotator Cuff Repair
The incidence of rotator cuff injuries is high, especially among the elderly. With the aging of the population, the number of surgical patients has increased significantly.
- Trial name
- NCT07311616
- Testing
- Prophylactic extensive shoulder release and capsular release, Arthroscopic rotator cuff repair
- Where
- China
- Volunteers
- 50 people
- Sponsor
- Beijing Jishuitan Hospital
Rotator Cuff Tear, Rotator Cuff Tears
Post-Market Clinical Follow-up (PMCF) Study of the Pitch-Patch for the Augmentation or Reinforcement of the Rotator Cuff
This is a clinical investigation study. It will verify the long-term safety and performance of the Pitch-Patch when implanted to reinforce partially repairable rotator cuff tears and used as described by the manufacturer's…
- Conditions
- Rotator Cuff Tear, Rotator Cuff Tears, Rotator Cuff Tears of the Shoulder, Rotator Cuff Injuries
- Trial name
- NCT05906004
- Testing
- Pitch-Patch
- Where
- United Kingdom
- Volunteers
- 37 people
- Sponsor
- Xiros Ltd
Arthroscopic Rotator Cuff Repair
Shoulder Anterior Capsular Block for Postoperative Analgesia in Arthroscopic Rotator Cuff Repair Surgery
Shoulder pain is frequently encountered in the medical field. Rotator cuff tears are the most common cause. Shoulder pain affects quality of life and delay rehabilitation programs.
- Trial name
- NCT06969625
- Testing
- (SHAC) block, (SSNB-ANB) block
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Zagazig University
Rotator Cuff Tear Repair, Interscalene Blocks
Preoperative Versus Postoperative Interscalene Block in Arthroscopic Rotator Cuff Repair
This study is evaluating whether the timing of an interscalene nerve block affects pain control and recovery after arthroscopic rotator cuff repair surgery.
- Conditions
- Rotator Cuff Tear Repair, Interscalene Blocks, Rotator Cuff Tears
- Trial name
- ISB-ARCR (NCT07689448)
- Where
- Turkey (Türkiye)
- Volunteers
- 42 people
- Sponsor
- Istinye University
Rotator Cuff Tear
A Randomized Controlled Trial on the Effectiveness of Early Versus Conservative Rehabilitation Following Rotator Cuff Repair
Background Rotator cuff tears (RCTs) are a common, costly, and often persistent musculoskeletal complaint, with an increasing number of shoulder pain patients undergoing surgical repair each year.
- Trial name
- NCT07324174
- Testing
- Group A, Therapeutic exercises, education and advice, Group B (Control Group)
- Where
- Saudi Arabia
- Volunteers
- 86 people
- Sponsor
- King Faisal Specialist Hospital & Research Center
Artroscopic Surgery, Pain Management
Suzetrigine for Analgesiain Arthroscopic Rotator Cuff Repair
The goal of this prospective is to determinate if Suzetrigine decreased de use of opioids in patients that undergo an arthroscopic rotator cuff repair.
- Conditions
- Artroscopic Surgery, Pain Management, Pain After Shoulder Surgery, Opioid Consumption
- Trial name
- SOAR (NCT07866638)
- Testing
- Suzetrigine (Journavx), Standard multimodal analgesia
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- University of Alabama at Birmingham
Rotator Cuff Repairs, Pain Management
The Effect of Multimodal Pain Regimen on Use of Narcotics After Rotator Cuff Tear Repair
The goal of this clinical trial is to understand which group of pain control medications work best in adults after rotator cuff surgery.
- Trial name
- NCT07076069
- Testing
- Multimodal Pain Regimen, Standard of Care Pain Regimen
- Where
- United States
- Volunteers
- 130 people
- Sponsor
- Montefiore Medical Center
Shoulder Surgery, Shoulder Pain
Evaluating Hemidiaphragmatic Paralysis With Prolonged Neural Blockade From an Interscalene Brachial Plexus Block
This prospective observational study aims to evaluate the incidence of hemidiaphragmatic paralysis in patients receiving interscalene brachial plexus nerve block with prolonged neural blockade.
- Conditions
- Shoulder Surgery, Shoulder Pain, Shoulder Injuries, Shoulder Arthritis
- Trial name
- NCT04209504
- Testing
- Ultrasound, Ropivacaine, Bupivacaine
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- Duke University
Rotator Cuff Tear
Superior Capsular Reconstruction vs. Partial Repair for Massive Rotator Cuff Tears
Little evidence exists to guide treatment in patients with massive irreparable rotator cuff tears (MRCTS). Arthroscopic partial rotator cuff repair (PRCR) has the longest record of use.
- Trial name
- SCR (NCT03617562)
- Testing
- Superior Capsular Reconstruction, Partial Repair
- Where
- 2 sites in Canada
- Volunteers
- 70 people
- Sponsor
- Sunnybrook Health Sciences Centre
Rotator Cuff Injuries
Effectiveness of Telerehabilitation as an Alternative to Outpatient Physiotherapy in the 1 Month After Arthroscopic Rotator Cuff Repair Surgery
The present study aims to verify whether telerehabilitation as an alternative to in-person treatment (both conducted by a physiotherapist) can be a valid option in terms of pain, recovery of the rom, shoulder functionality…
- Trial name
- NCT06744218
- Testing
- Standard Treatment, Experimental Treatment
- Where
- 2 sites in Italy
- Volunteers
- 46 people
- Sponsor
- Istituto Ortopedico Rizzoli
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