Clinical trials: Rotator Cuff Tears, open to volunteers
Orthopedic Disorder
SupraScapular Cuff Study: Assessing the Effects of Size and Type of Rotator Cuff Tear on Suprascapular Nerve Function
The primary objective of the study is to determine in adult patients with a rotator cuff tear, what size and pattern of rotator cuff tear would result in damage to the suprascapular nerve. The secondary objectives are 1.
- Trial name
- SSCuFF (NCT06002009)
- Testing
- MRI, Nerve conduction study
- Where
- United Kingdom
- Volunteers
- 250 people
- Sponsor
- University Hospitals of North Midlands NHS Trust
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
Rotator Cuff Tears
RC Repair Versus Subacromial Balloon Spacer in Older Adults
The purpose of this pilot study is to assess the feasibility of a full randomized trial design.
- Trial name
- NCT05788250
- Testing
- Subacromial spacer implantation, Rotator cuff repair
- Volunteers
- 32 people
- Sponsor
- Panam Clinic
Labral Tear, Glenoid, Femoral Acetabular Impingement
Blood Flow Restriction Following Hip Arthroscopy
This study will be a prospective randomized, double-blinded, placebo-controlled trial of patients undergoing primary hip arthroscopy for FAIS and/or labral pathology.
- Trial name
- NCT04113759
- Testing
- Blood Flow Restriction Rehabilitative Therapy
- Where
- United States
- Volunteers
- 56 people, healthy volunteers welcome
- Sponsor
- Rush University Medical Center
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
Rotator Cuff Tears
Acellular Matrix From Human Dermis in Combination With Orthobiologic Stimuli for Augmentation of Massive Rotator Cuff Tears
The use of biologic acellular matrices for the surgical augmentation of rotator cuff lesions has greatly expanded inrecent years.
- Trial name
- MODA (NCT05855759)
- Testing
- Acellular Dermal Matrix, Acellular Dermal Matrix with autologous orthobiologics
- Where
- Italy
- Volunteers
- 72 people
- Sponsor
- Istituto Ortopedico Rizzoli
Rotator Cuff Tear, Rotator Cuff Injury
Rotator Cuff Tendon Repair With FiberLocker System Patch Augmentation
The overall objective of this clinical investigation is to assess the safety and efficacy of full-thickness arthroscopic rotator cuff repairs augmented with the FiberLocker System for the subjects.
- Conditions
- Rotator Cuff Tear, Rotator Cuff Injury, Rotator Cuff Rupture
- Trial name
- FIBERLOCK (NCT07005063)
- Testing
- FiberLocker® System (encompassing SpeedPatch® PET and FiberLocker Instrument® SN)
- Where
- Switzerland
- Volunteers
- 50 people
- Sponsor
- ZuriMED Technologies AG
Rotator Cuff Tear Surgical Repair
Clinical Trial to Compare Clinical and Functional Results of the Augmentation of Supraspinatus Tears With the Long Head of the Biceps Brachii Tendon
The goal of this clinical trial is to reduce the risk for re-tear in rotator cuff surgeries and improve clinical results in a working age population.
- Trial name
- NCT07657689
- Testing
- Augmented supraspinatus repair, Convencional Supraspinatus tear repair
- Volunteers
- 90 people
- Sponsor
- HOSPITAL FRATERNIDAD MUPRESPA HABANA
Rotator Cuff Tears
Effect of Central Sensitization on Response to Physical Therapy in Patients With Partial Supraspinatus Tear
This prospective observational study aims to investigate whether central sensitization influences the response to physical therapy in patients with partial supraspinatus tendon tears.
- Trial name
- NCT07664137
- Testing
- Standard Physical Therapy and Rehabilitation
- Volunteers
- 60 people
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Opioid Use, Pain
Hip Arthroscopy Postoperative Opioid Demands
This study will be a prospective, single-blinded, randomized controlled trial (RCT), investigating the influence of the number of opioid pills prescribed following primary hip arthroscopy.
- Conditions
- Opioid Use, Pain, Femoral Acetabular Impingement, Labral Tear, Glenoid
- Trial name
- NCT04094701
- Testing
- Control Group Regimen, Opioid reduced regimen
- Where
- United States
- Volunteers
- 170 people, healthy volunteers welcome
- Sponsor
- Rush University Medical Center
Osteoarthritis Shoulder, Rotator Cuff Tears
DenCT Shoulder Bone Quality Evaluation
The objective of the study is to evaluate the preoperative bone quality assessment based on CT to later establish a scale for the decision of stemless shoulder arthroplasty.
- Trial name
- NCT06032416
- Testing
- Preoperative CT Scan
- Where
- Japan
- Volunteers
- 200 people
- Sponsor
- Zimmer Biomet
Rotator Cuff Tears, Anatomic Total Shoulder Arthroplasty
Innovating Physical Therapy: A Pilot Study on Band Connect's Impact on Compliance, Satisfaction, and Revenue
Participants are being invited to take part in this research study because you will be undergoing total shoulder replacement or rotator cuff repair and will be participating in physical therapy rehabilitation following the…
- Conditions
- Rotator Cuff Tears, Anatomic Total Shoulder Arthroplasty, Reverse Total Shoulder Arthroplasty
- Trial name
- NCT06733480
- Testing
- Band Connect
- Where
- United States
- Volunteers
- 499 people
- Sponsor
- University Hospitals Cleveland Medical Center
Rotator Cuff Arthropathy
Prosthesis Versus Active Exercise Program in Patients With Rotator Cuff Arthropathy
Reverse shoulder arthroplasty (RSA) is a well-established treatment for rotator cuff arthropathy. However, the effectiveness of RSA has not been compared to non-surgical treatment in a randomised controlled trial.
- Trial name
- REACT (NCT04864158)
- Testing
- TSA-group, Exercise-group
- Where
- 8 sites in Denmark, Estonia and 2 more
- Volunteers
- 102 people
- Sponsor
- University of Aarhus
Rotator Cuff Injuries, Rotator Cuff Tears
Slow and Accelerated Rehabilitation Protocols
Latissimus dorsi transfer is an established treatment option with favorable results in massive, irreparable rotator cuff tears, however, it is controversial if earlier motion is detrimental or beneficial to the postoperative goal…
- Conditions
- Rotator Cuff Injuries, Rotator Cuff Tears, Pain, Shoulder
- Trial name
- NCT05450510
- Testing
- Accelerated (ACCEL) protocol group, Slow (SLOW) protocol group
- Where
- Turkey (Türkiye)
- Volunteers
- 38 people
- Sponsor
- Hacettepe University
Rotator Cuff Tears, Rotator Cuff Injuries
Analysis of Sleep & Recovery Following Rotator Cuff Repair Surgery
Postoperative recovery following a rotator cuff repair surgery can be challenging. In particular, sleeping is difficult given the restrictions of the operative shoulder.
- Conditions
- Rotator Cuff Tears, Rotator Cuff Injuries, Shoulder Pain, Shoulder Injuries
- Trial name
- NCT06625723
- Testing
- Standard postoperative care, Surgical Recovery Systems Sleep Aid
- Volunteers
- 60 people
- Sponsor
- New York Presbyterian Hospital
Massive Rotator Cuff Tear
Effects Of Biceps Transposition Without Tenotomy For Augmentation Of Massive Rotator Cuff Repairs
This prospective, single-arm interventional study will evaluate the effects of long head of the biceps tendon (LHBT) transposition without tenotomy as an augmentation technique for arthroscopic partial repair in adults with…
- Trial name
- ROTATORCUFF (NCT07375277)
- Testing
- LHBT Transposition Augmentation
- Where
- Turkey (Türkiye)
- Volunteers
- 35 people
- Sponsor
- Balikesir Ataturk City Hospital
Calcific Tendinitis of Shoulder
The Effect of Doppler Ultrasound on Calcified Tendinitis
Calcific tendinitis of the shoulder, is a self-limiting disease characterized by the deposition of calcium phosphate crystals in the rotator cuff tendons.
- Trial name
- NCT06503302
- Testing
- ultrasound Doppler function detection
- Where
- Taiwan
- Volunteers
- 100 people
- Sponsor
- Taipei Medical University Shuang Ho Hospital
Partial Rotator Cuff Tears (PRCTs)
High-frequency Short-course Extracorporeal Shock Wave Therapy for Partial Rotator Cuff Tears: Study Protocol for a Multicenter, Randomized, Controlled Trial
This is a multicenter, randomized controlled clinical study exploring three different extracorporeal shock wave therapy (ESWT) regimens for patients with partial rotator cuff tears, a common cause of chronic shoulder pain and…
- Trial name
- NCT07673055
- Testing
- Arm 1 Intervention Name: High-frequency short-course extracorporeal shock wave therapy Arm 2 Intervention Name: High-frequency intensive extracorporeal shock wave therapy Arm 3 Intervention Name: Conv
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- Peking University Third Hospital
Shoulder Instability, Frozen Shoulder
Virtual Reality Rehabilitation for Shoulder Pathologies
Most rehabilitation protocols require patients to train the affected limbs with high regularity, following repetitive cycles of exercises, in order to recover mobility and strength.
- Conditions
- Shoulder Instability, Frozen Shoulder, Rotator Cuff Tears
- Trial name
- NCT06963983
- Testing
- Rehabilitation using virtual reality
- Where
- Switzerland
- Volunteers
- 15 people
- Sponsor
- La Tour Hospital
Rotator Cuff Injury
Biceps Lasso Loop and Self- Locking Tenodesis Alongside Repair of Rotator Cuff Tears: Randomised Controlled Trial Study Protocol (BLAST 1)
The aim of this study is to compare the clinical results and complications of self-locking biceps tenodesis and double 360 lasso loop biceps tenodesis for the treatment of long chief of biceps or superior labrum…
- Trial name
- BLAST 1 (NCT06774820)
- Testing
- self-blocking tenodesis, arthroscopic tenodesis
- Where
- France
- Volunteers
- 100 people
- Sponsor
- Clinique Générale dAnnecy