Clinical trials: Full Thickness Rotator Cuff Tear
Shoulder Injuries
Rotator Cuff Repair With Arthroscopic Acromioplasty (Shaving the Acromion Bone) Versus Repair Without Acromioplasty
Surgical repair of full-thickness tears of the rotator cuff is a controversial issue, with several procedures currently being used to treat the tear.
- Trial name
- NCT00664794
- Testing
- without acromioplasty, with acromioplasty
- Where
- 2 sites in Canada
- Volunteers
- 50 people
- Sponsor
- Ottawa Hospital Research Institute
Rotator Cuff Tear
Types of Fixation in Arthroscopic Rotator Cuff Repair
The study will identify if there is a difference of quality of life after surgery between two techniques used in surgery. The two different techniques are either the Single Row Fixation or the Double Row Fixation.
- Trial name
- NCT00508183
- Testing
- single row, double row fixation
- Where
- Canada
- Volunteers
- 90 people, healthy volunteers welcome
- Sponsor
- Ottawa Hospital Research Institute
Full Thickness Rotator Cuff Tear
Clinical and Structural Outcome After Early Repair of the Traumatic Rotator Cuff Tear
The optimal timing for surgical repair of traumatic rotator cuff tears is controversial. Today there are no prospective studies investigating the short to mid-term outcome after early arthroscopic repair of traumatic rotator cuff…
- Trial name
- NCT01557309
- Where
- Sweden
- Volunteers
- 60 people
- Sponsor
- Helsingborgs Hospital
Full Thickness Rotator Cuff Tears
Early Mobilization Following Mini-Open Rotator Cuff Repair
The primary objective of this study is to determine if early active range of motion after mini-open rotator cuff repair in adults results in improved shoulder range of motion at 6 weeks and 3 months after surgery.
- Trial name
- NCT01741272
- Testing
- Sling, No sling
- Where
- Canada
- Volunteers
- 189 people
- Sponsor
- University of Alberta
Full Thickness Rotator Cuff Tear
Effectiveness Study of Postoperative Rotator Cuff Repair Rehabilitation
There are very few level 1 or level 2 evidence studies that examine postoperative rehabilitation of rotator cuff repair and shoulder arthroplasty.
- Trial name
- NCT01819909
- Testing
- Postoperative Jackins Exercise Protocol, Postoperative Pulleys Exercise Protocol
- Where
- United States
- Volunteers
- 53 people
- Sponsor
- Orthopedic Institute, Sioux Falls, SD
Cuff Rotator Full Thickness Tear, Cuff Rotator Syndrome
Neuropathy of the Suprascapular Nerve Before and After Reconstruction of the Cuff
The suprascapular nerve innervates the musculi supra- and infraspinatus, which, as part of the rotator cuff, allow lifting and external rotation in the shoulder joint. Damage to this nerve can lead to pain and functional deficit.
- Trial name
- Neurospura (NCT03953339)
- Testing
- Release or no release of the suprascapular nerve
- Where
- Switzerland
- Volunteers
- 20 people
- Sponsor
- Balgrist University Hospital
Full Thickness Rotator Cuff Tear
Enhanced Function and Quality of Life Following 5 Months of Exercise Therapy for Patients With Rotator Cuff Tears
This study aims to evaluate the effect of 5 months of exercise therapy for patients with irreparable rotator cuff tears.
- Trial name
- NCT02740946
- Testing
- Exercise therapy
- Where
- Denmark
- Volunteers
- 30 people
- Sponsor
- Northern Orthopaedic Division, Denmark
Rotator Cuff Tear, Shoulder Impingement Syndrome
Arthroscopic Rotator Cuff Repair of Full Thickness Tears With and Without Arthroscopic Acromioplasty
Surgical repair of full thickness tears of the rotator cuff is a controversial issue, with several procedures currently being used to treat the tear.
- Trial name
- NCT00290888
- Testing
- Acromioplasty
- Where
- Canada
- Volunteers
- 86 people
- Sponsor
- Panam Clinic
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
Full Thickness Rotator Cuff Tear
BioFiber Scaffold Post-Market Observational Study
The aim of this study is to collect and report data from a consecutive series of patients implanted with these products as part of a post-market surveillance plan for CE Mark approval in the European Union.
- Trial name
- NCT01849458
- Testing
- BioFiber
- Where
- 3 sites in United States, France
- Volunteers
- 50 people
- Sponsor
- Stryker Trauma and Extremities
Rotator Cuff Tears
Clinical Trial on the Effect of the Flexible Suturing System With Anchors (FSSA) in Full-thickness Rotator Cuff Tendon Tears
The purpose of this research study is to evaluate tendon healing when using the Flexible Suturing System with Anchors (FSSA) to surgically repair full-thickness rotator cuff tendon tears.
- Trial name
- NCT06868108
- Testing
- Flexible Suturing System with Anchors (FSSA)
- Where
- 3 sites in United States
- Volunteers
- 100 people
- Sponsor
- Integrity Orthopaedics, Inc.
Rotator Cuff Tears
Neuromuscular Electrical Stimulation on Humeral Adductors in Subjects With Rotator Cuff Tear: an Observational Study
The teres major and pectoralis major are adductors and may play a compensatory role for deficit in rotator cuff function. The investigators aim to (1) determine the effects of neuromuscular electrical stimulation (NMES) on the…
- Trial name
- NCT05879003
- Testing
- novel brace with neuromuscular electrical stimulation, scapular and adductor exercise
- Where
- Taiwan
- Volunteers
- 120 people
- Sponsor
- National Taiwan University Hospital
Full-thickness Rotator Cuff Tear
Efficacy of Continuous Infusion Ropivacaine Interscalene Blocks
Arthroscopic rotator cuff repair is a common and painful procedure routinely performed on an outpatient basis. Postoperative pain control regimens can include narcotic pain medicine, non-steroidal anti-inflammatory medications…
- Trial name
- NCT02462382
- Testing
- Arthroscopic Rotator Cuff Repair, Ropivacaine, Saline
- Where
- United States
- Volunteers
- 51 people
- Sponsor
- Orlando Health, Inc.
Partial Thickness Rotator Cuff Tears
Arthroscopic Biological Augmentation With Subacromial Bursa for Bursal Side Partial-thickness Rotator Cuff Tears
The investigators aimed to compare the results of acromioplasty + arthroscopic debridement and acromioplasty + augmentation with subacromial bursa.
- Trial name
- NCT05823428
- Testing
- Augmentation with subacromial bursa + acromioplasty, Rotator cuff debridement + acromioplasty
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Rotator Cuff Tear
A Randomized Clinical Trial Comparing Open to Mini-Open Rotator Cuff Repair for Full-Thickness Rotator Cuff Tears.
This study compares standard open rotator cuff repair versus arthroscopic mini-open rotator cuff repair by measuring the disease-specific quality of life at 2 years in patients with full thickness rotator cuff tears.
- Trial name
- NCT00251147
- Testing
- Open acromioplasty with rotator cuff repair, Arthroscopic acromioplasty with mini-open repair
- Where
- 4 sites in Canada
- Volunteers
- 73 people
- Sponsor
- University of Calgary
Full Thickness Rotator Cuff Tear
A Pilot Cohort Study of Surgical and Non-surgical Management of Rotator Cuff Tears
This project will involve planning and implementing a two-arm prospective pragmatic cohort clinical trial in patients with known rotator cuff tears.
- Trial name
- NCT03021733
- Testing
- Operative management
- Volunteers
- 222 people, healthy volunteers welcome
- Sponsor
- University of Michigan
Full-thickness Rotator Cuff Tear
Dermal Allograft Augmentation of Large and Massive Rotator Cuff Tears
The purpose of this study is to compare postoperative healing of large and massive rotator cuff tears with preoperative MRI confirmed fatty infiltration stage II and higher repaired with or without dermal allograft augmentation…
- Trial name
- NCT05981833
- Testing
- Repair with DAA (dermal allograft augmentation)
- Where
- 4 sites in United States
- Volunteers
- 120 people
- Sponsor
- Arthrex, Inc.
Rotator Cuff Tear
InSpace™ System in Comparison to Best Repair of Massive Rotator Cuff Tear
This is a post-marketing study to further assess the safety and effectiveness of the InSpace™ device implantation in comparison to surgical repair of full thickness Massive Rotator Cuff Tear .
- Trial name
- NCT02211183
- Testing
- Best Repair of torn Rotator Cuff, InSpace™ system
- Where
- Spain
- Volunteers
- 4 people
- Sponsor
- OrthoSpace Ltd.
Arm Injuries
Pilot Study to Evaluate the Restore Orthobiologic Implant in Rotator Cuff Tear Repair
Primary Endpoints: Comparative evaluation of any differences between the two groups in change from baseline to the 3-month time point in terms of: Functional recovery (patient-based) - using the Oxford Shoulder Score.
- Trial name
- NCT00208338
- Testing
- RESTORE SIS Patch, Rotator cuff repair
- Where
- 2 sites in Belgium, United Kingdom
- Volunteers
- 33 people
- Sponsor
- DePuy International
Rotator Cuff, Subacromial Impingement Syndrome
Comparison of Strength and Constant Score Pre- and Post-Subacromial Injection for Full Thickness Rotator Cuff Tears
Clinical manifestations of rotator cuff tear include shoulder pain, weakness, and stiffness. The level of pain is often a limiting factor when assessing shoulder range of motion and strength pre-operatively.
- Trial name
- NCT02693444
- Testing
- Lidocaine, Saline
- Sponsor
- Rush University Medical Center