Clinical trials: Rotator Cuff Tears, open to volunteers
Shoulder Impingement Syndrome, Rotator Cuff Injuries
The Role of Pectoralis Minor Tightness in the Development of Rotator Cuff Tears
This study investigates whether tightness of a small chest muscle called the pectoralis minor is associated with the development of partial rotator cuff tears in the shoulder.
- Conditions
- Shoulder Impingement Syndrome, Rotator Cuff Injuries, Pectoralis Minor Tightness, Pectoralis Minor Muscle Tension
- Trial name
- PMinor-Rotator (NCT07228936)
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people, healthy volunteers welcome
- Sponsor
- Gazi University
Primary Osteoarthritis, Secondary Osteoarthritis
Clinical and Radiological Outcomes of Medacta Shoulder System FR
This is a post-marketing surveillance on Medacta Shoulder System
- Conditions
- Primary Osteoarthritis, Secondary Osteoarthritis, Rotator Cuff Tear Arthropathy, Rheumatoid Arthritis Shoulder
- Trial name
- NCT05926622
- Where
- France
- Volunteers
- 200 people
- Sponsor
- Medacta International SA
Supraspinatus Tear
Treatment of the Biceps With Concomitant Supraspinatus Tears
The long head of the biceps (LHB) tendon is thought to be a common source of shoulder pain and dysfunction in patients with rotator cuff pathology.
- Trial name
- NCT05660031
- Testing
- LHB Tenotomy, LHB Tenodesis
- Where
- 4 sites in United States, Canada and 1 more
- Volunteers
- 180 people
- Sponsor
- La Tour Hospital
Rotator Cuff Tears, Rotator Cuff Injuries
Estradiol Supplementation and Rotator Cuff Repair
Rotator cuff tears in the shoulder are common causes of pain and disability, often fail to heal with surgery, and tears, worse outcomes after surgery, and failure of healing are associated with estradiol deficiency.
- Conditions
- Rotator Cuff Tears, Rotator Cuff Injuries, Rotator Cuff Syndrome, Menopause Related Conditions
- Trial name
- ESTRCR (NCT06318403)
- Testing
- Transdermal estrogen, Rotator Cuff Repair Surgery
- Volunteers
- 58 people
- Sponsor
- University of Utah
Rotator Cuff Tear
Preoperative Central Sensitization and Postoperative Outcomes After Arthroscopic Rotator Cuff Repair
This prospective observational study aims to investigate the effect of preoperative central sensitization on postoperative clinical outcomes in patients undergoing arthroscopic rotator cuff repair.
- Trial name
- ARCS (NCT07667257)
- Testing
- Arthroscopic Rotator Cuff Repair
- Volunteers
- 50 people
- Sponsor
- Medipol University
Rotator Cuff Tears
Biomarkers to Predict Rotator Cuff Repair Healing on Postoperative MRI
Rotator cuff repair healing is highly variable with healing failure rates ranging from 11 to 94%. To this date, there are no specific biomarkers in shoulder tissues that can be associated with rotator cuff healing after surgery.
- Trial name
- NCT07781553
- Testing
- MRN
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- Joseph W. Galvin
Rotator Cuff Injury, Rotator Cuff Tears
Blood Flow Restriction Versus Standard Exercise After Rotator Cuff Repair
The goal of this clinical trial is to determine the effectiveness of postoperative standard exercises with blood flow restriction therapy (BFRT) versus standard exercises alone on shoulder muscle strength and mass in participants…
- Conditions
- Rotator Cuff Injury, Rotator Cuff Tears, Rotator Cuff Repair
- Trial name
- S-TRONGER (NCT06788327)
- Testing
- Standard rehabilitation, Blood Flow Restriction Therapy
- Where
- Chile
- Volunteers
- 50 people
- Sponsor
- University of Valencia
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
Rotator Cuff Tears
Lower Trapezius Transfer vs Bridging Reconstruction
The goal of this clinical trial is to compare the bridging reconstruction technique vs the lower trapezius tendon transfer in patients with massive irreparable rotator cuff tears.
- Trial name
- NCT05925881
- Testing
- Surgical Repair of Large to Massive Rotator Cuff Tears
- Where
- Canada
- Volunteers
- 60 people
- Sponsor
- Nova Scotia Health Authority
Rotator Cuff Injuries
Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears
The purpose of the study is to assess whether the REGENETEN™ Bioinductive Implant allows patients to get back to their everyday activities quicker than if the tendon is repaired by the standard repair technique 'Completion and…
- Trial name
- IMPACT (NCT05444465)
- Testing
- Isolated Bioinductive Repair, Completion and Repair
- Where
- 20 sites in United States, Australia and 4 more
- Volunteers
- 234 people
- Sponsor
- Smith & Nephew, Inc.
Rotator Cuff Tears (RCTs)
Smallest Worthwhile Effect of Rotator Cuff Repair and Supervised Exercise
The goals of this observational study are (1) to determine the smallest worthwhile effect of rotator cuff repair surgery compared to exercise therapy in rotator cuff patients; (2) to determine the smallest worthwhile effect of…
- Trial name
- NCT07779876
- Volunteers
- 104 people
- Sponsor
- Kırklareli University
Lesion of Long Head of Biceps, SLAP Lesion
Reliability and Accuracy of a New Clinical Test for Biceps Lesions
The purpose of this study is to evaluate the accuracy and reliability of a new physical examination test (referred to as Said's test) for diagnosing injuries to the biceps tendon in the shoulder, specifically lesions of the long…
- Conditions
- Lesion of Long Head of Biceps, SLAP Lesion, Biceps Tendinopathy, Rotator Cuff Tear
- Trial name
- NCT07531225
- Volunteers
- 144 people
- Sponsor
- Assiut University
Rheumatoid Arthritis, Osteoarthritis Shoulder
Tornier HRS (Humeral Reconstruction System) Study (REVIVE)
This is an international, single arm, multicenter, prospective follow-up, non-significant risk, Post-Market Clinical Follow-up (PMCF) study.
- Conditions
- Rheumatoid Arthritis, Osteoarthritis Shoulder, Fractures Humerus, Avascular Necrosis
- Trial name
- REVIVE (NCT05500066)
- Testing
- Tornier HRS (HUMERAL RECONSTRUCTION SYSTEM) shoulder system
- Where
- 4 sites in United States
- Volunteers
- 110 people
- Sponsor
- Stryker Trauma and Extremities
Partial Supraspinatus Tear, Rotator Cuff Tears (RCTs)
Platelet-Rich Plasma for Partial Rotator Cuff Tears
The goal of this clinical trial is to learn whether platelet-rich plasma (PRP) injection, made from a participant's own blood, can help heal the tendon and improve shoulder symptoms in people with partial tears of the…
- Conditions
- Partial Supraspinatus Tear, Rotator Cuff Tears (RCTs), Rotator Cuff Injury
- Trial name
- OPTIMISE (NCT07659600)
- Testing
- Platelet-Rich Plasma (PRP) Injections
- Volunteers
- 100 people
- Sponsor
- Universidade Nova de Lisboa
Rotator Cuff Tears
The Effect of Self-rehabilitation Using Communication APP After Arthroscopic Surgery for Rotator Cuff Tear
The purpose of this study was to assess the clinical effect of a mobile application supporting home-based rehabilitation for the patients after arthroscopic rotator cuff repair.
- Trial name
- NCT05102968
- Testing
- Home-based rehabilitation supporting with the mobile application, Supervised rehabilitation by the therapist
- Where
- Taiwan
- Volunteers
- 60 people
- Sponsor
- Kaohsiung Veterans General Hospital.
Humeral Fracture, Proximal, Glenohumeral Osteoarthritis
RETRO-PROSPECTIVE POSTMARKET CLINICAL STUDY FOR FX SHOULDER SOLUTIONS SHOULDER SYSTEMS
This study takes place in the framework of the PostMarket Clinical Follow-up plan of the Shoulder Systems commercialized by FX SHOULDER SOLUTIONS. The included cases will be followed for 10 years after index surgery.
- Conditions
- Humeral Fracture, Proximal, Glenohumeral Osteoarthritis, Avascular Necrosis of the Head of Humerus, Rotator Cuff Tear
- Trial name
- NCT07558590
- Testing
- Shoulder arthroplasty
- Where
- 22 sites in France, Monaco
- Volunteers
- 1,004 people
- Sponsor
- FX Solutions
Rotator Cuff Tears of the Shoulder
Integrity Implant System Post Market Clinical Follow-Up Study
The study design is a prospective, multi-center, single-arm, non-randomized post market clinical follow-up study to confirm the performance, safety and clinical benefit of the Integrity Implant System when used for rotator cuff…
- Trial name
- NCT06741527
- Testing
- Integrity Implant System
- Where
- 9 sites in United States
- Volunteers
- 150 people
- Sponsor
- Anika Therapeutics, Inc.
Supraspinatus Tear
Novel Treatment for Rotator Cuff Tears
The focus of this study is to examine changes in pain scores, strength, and range of motion over time following an ultrasonic tenotomy on a partial tear (<50%) of the supraspinatus tendon of the rotator cuff.
- Trial name
- NCT05590494
- Testing
- Ultrasonic tenotomy
- Where
- United States
- Volunteers
- 15 people
- Sponsor
- Mayo Clinic
Arthroplasty, Replacement
SMR Stemless Reverse vs SMR Reverse Shoulder System
The SMR Stemless Reverse is intended for total, primary shoulder joint replacement by reducing pain and restoring shoulder articular mobility function.
- Trial name
- NCT04697004
- Testing
- Investigational Arm: SMR Stemless Reverse, Control Arm: SMR Reverse Shoulder System
- Where
- 13 sites in United States
- Volunteers
- 200 people
- Sponsor
- Limacorporate S.p.a
Osteoarthritis, Osteosarcoma
Clinical Orthopaedic Data Bank (Acute and Chronic)
Data involving orthopaedic conditions and rehabilitation aspects of musculoskeletal and neuromuscular disorders will be collected and stored as part of the normal clinical care of patients seen in the University of Florida (UF)…
- Conditions
- Osteoarthritis, Osteosarcoma, Scoliosis, Cerebral Palsy
- Trial name
- NCT00411060
- Where
- United States
- Volunteers
- 10,000 people
- Sponsor
- University of Florida