Clinical trials: Rotator Cuff Repairs
Rotator Cuff Injury, Pain
Pre-emptive Opioid Treatment to Prevent Rebound Pain After Arthroscopic Rotator Cuff Repair and/or Acromioplasty Under General Anesthesia and Interscalene Block
Arthroscopic shoulder rotator cuff repair and acromioplasty are associated with severe postoperative pain. The interscalene block (ISB) is commonly used for this type of surgery, providing analgesia by anesthetizing the nerves…
- Trial name
- NCT02939209
- Testing
- Hydromorphone Hcl 2Mg Tab
- Where
- 2 sites in Canada
- Volunteers
- 73 people, healthy volunteers welcome
- Sponsor
- Vishal Uppal
Rotator Cuff Tear, Acromial Spur
Study Comparing Patient Function and Satisfaction With Arthroscopic Subacromial Decompression Before and After Repair of Complete Rotator Cuff Tears
The investigators aim to establish whether completing a subacromial decompression before or after repair of a complete rotator cuff tear has any clinical significance.
- Trial name
- NCT01430598
- Testing
- Rotator Cuff Repair and Subacromial Decompression, Questionnaire
- Where
- 2 sites in United States
- Volunteers
- 100 people
- Sponsor
- Ascension Health
Analgesia, Patient-Controlled, Brachial Plexus Block
Comparison of Using CIBPB With or Without IV-PCA After Arthroscopic Rotator Cuff Repair
The goal of this study is to compare the continuous brachial plexus block with or without intravenous patient controlled analgesia(PCA) in patients undergoing arthroscopic rotator cuff repair, in terms of quality of recovery…
- Conditions
- Analgesia, Patient-Controlled, Brachial Plexus Block, Arthroscopic Rotator Cuff Repair
- Trial name
- NCT05691101
- Testing
- CISB with IV PCA group, CISB group
- Where
- South Korea
- Volunteers
- 80 people
- Sponsor
- Seoul National University Bundang Hospital
Full-thickness Rotator Cuff Tear
PEMF as Adjunctive Treatment Following Surgical Repair of Full Thickness Rotator Cuff Tears
The primary objective of this study is to prospectively determine, at 12 months post-surgical repair of full thickness rotator cuff tears, the safety and efficacy of treating full thickness rotator cuff repairs with pulsed…
- Trial name
- RCStim (NCT03339492)
- Testing
- RCStim Model 1114
- Where
- 23 sites in United States
- Volunteers
- 377 people
- Sponsor
- Orthofix Inc.
Rotator Cuff Tear, Rotator Cuff Injury
Buprenorphine Transdermal Patches in Arthroscopic Rotator Cuff Repair
Arthroscopic rotator cuff repair is associated with poor post-operative pain management. The multimodal analgesic scheme (oral non-steroidal anti-inflammatory drugs associated with oral opioids) currently used according to the…
- Conditions
- Rotator Cuff Tear, Rotator Cuff Injury, Analgesics, Opioid, Buprenorphine
- Trial name
- NCT03380533
- Testing
- Buprenorphine, Multimodal Oral Scheme, Tramadol
- Where
- Argentina
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Hospital Italiano de Buenos Aires
Rotator Cuff Repair, Ankle Arthroplasty or Arthrodesis
Ultrasound-Guided Percutaneous Peripheral Nerve Stimulation: A Department of Defense Funded Pragmatic Clinical Trial
Postoperative pain is usually treated with opioids that have undesirable and sometimes dangerous side effects (e.g., vomiting and respiratory depression)-and yet over 80% of patients still experience inadequate pain relief.
- Conditions
- Rotator Cuff Repair, Ankle Arthroplasty or Arthrodesis, Hallux Valgus (Bunion) Resection
- Trial name
- NCT04713098
- Testing
- Peripheral Nerve Stimulation
- Where
- 6 sites in United States
- Volunteers
- 250 people
- Sponsor
- University of California, San Diego
Rotator Cuff Tears
Biomodulating Rotator Cuff Healing - A Proof of Concept Trial
Novel concepts in quantum biology of rotator cuff repair and author's novel findings on biomodulation inspired us to design a pragmatic non-pharmacological add-on rehabilitation protocol that may potentially decrease retear rates…
- Trial name
- BIOHACK (NCT04618484)
- Testing
- Biomodulation (non-pharmacological)
- Where
- France
- Volunteers
- 146 people
- Sponsor
- Clinique Générale dAnnecy
Shoulder Pain
Rotator Cuff Pathway
Rotator cuff surgery is mostly performed on an outpatient basis, and many patients still experience moderate to severe pain after surgery, despite the use of regional anesthesia and opioids.
- Trial name
- NCT03717753
- Testing
- Pathway
- Where
- United States
- Volunteers
- 140 people
- Sponsor
- Hospital for Special Surgery, New York
Brachial Plexus Injury
Incidence of Brachial Plexus Injury After Rotator Cuff Repair With Continuous Interscalene Block
Brachial plexus injury after shoulder surgery with continuous interscalene block is 2.4% at 1 month and 0% at 6 months, but may be higher with a systematic postoperative neurological examination.
- Trial name
- NCT01334632
- Testing
- Continuous interscalene block, PCA morphine
- Where
- Switzerland
- Volunteers
- healthy volunteers welcome
- Sponsor
- Centre Hospitalier Universitaire Vaudois
Rotator Cuff Syndrome
Prospective Randomized Comparative Study of Outcome of Subscapularis Tear
The purpose of this study was to report actual percentage of subscapularis tear in concomitant with supraspinatus tendon tear (with or without infraspinatus tear) and investigate the amount of contribution of subscapularis repair…
- Trial name
- NCT01996904
- Testing
- arthroscopic repair, arthroscopic debridement
- Where
- South Korea
- Volunteers
- 191 people
- Sponsor
- CM Chungmu Hospital
Rotator Cuff Tears
Platelet Rich Plasma on Rotator Cuff Repair
Repair of the rotator cuff has high rates of re-rupture (20-54%), despite good clinical results. Several ways to improve the healing tendon-bone are currently studied, among them the most used is the use of growth factors.
- Trial name
- PRP (NCT01029574)
- Testing
- Platelet rich plasma
- Where
- 2 sites in Brazil
- Volunteers
- 54 people
- Sponsor
- University of Sao Paulo
Rotator Cuff Tear
Vascular Changes of Rotator Cuff Repair Augmented With a Whole Blood Fibrin Clot
The goal of this study is to assess whether undergoing surgical repair of the rotator cuff with the additional intervention of whole blood fibrin clot will improve rotator cuff vascularization at the bone-tendon interface repair…
- Trial name
- NCT03577379
- Testing
- Whole Blood Fibrin Clot
- Where
- United States
- Volunteers
- 53 people
- Sponsor
- Santa Barbara Cottage Hospital
Rotator Cuff Tear, Fatty Atrophy
Efficacy of an Amniotic Fluid Derived Allograft, (FlōGraft®) in Rotator Cuff Repairs: A Prospective Study
Rotator Cuff (RC) repair will be augmented with the injection of a human amniotic fluid derived allograft at the repair interface junction.
- Trial name
- NCT03379324
- Testing
- Superiority of augmented repairs, Fat degeneration of supraspinatus muscle
- Where
- United States
- Volunteers
- 260 people, healthy volunteers welcome
- Sponsor
- Applied Biologics, LLC
Rotator Cuff Injury
Post-Operative Quality of Life Evaluation for Different Anesthesia Techniques for Arthroscopic Shoulder Surgery
Randomized controlled trial on efficacy of single injection or continuous interscalene brachial plexus block on analgesia in patients having outpatient rotator cuff surgery.
- Trial name
- NCT01355757
- Testing
- Baxter INFUSOR System, Single Injection of Local Anesthetic
- Where
- United States
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- St. Luke's-Roosevelt Hospital Center
Disorder of Rotator Cuff
Interscalene and Combined Supra Scapular and Axillary Nerve Blocks in Rotator Cuff Repair
Primary objective of this study is to prospectively compare and evaluate efficacy as well as note side effects of the interscalene block and combined suprascapular and axillary nerve block for ambulatory arthroscopic rotator cuff…
- Trial name
- NCT01730573
- Testing
- interscalene block, Suprascapular and Axillary nerve block
- Where
- 2 sites in Canada
- Volunteers
- 60 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Rotator Cuff Tears
Comparison Between Arthroscopic Debridement and Repair for Partial-thickness Rotator Cuff Tears
The purpose of this study is to conduct a prospective randomized controlled trial to compare the effects of arthroscopic debridement and repair for Ellman grade II bursal-side partial-thickness rotator cuff tears.The hypothesis…
- Trial name
- NCT04710966
- Testing
- arthroscopic debridement, arthroscopic repair
- Where
- China
- Volunteers
- 179 people
- Sponsor
- The Affiliated Hospital of Qingdao University
Shoulder Lesions
Analgesic Efficacy of US-Guided Interscalene Block Versus Supraclavicular Block for Ambulatory Arthroscopic Rotator Cuff Repair
Ultrasound-guided interscalene block (ISB) is the reference technique for pain control after ambulatory upper limb surgery, but supraclavicular block (SCB) is an alternative procedure.
- Trial name
- BISBSC (NCT03743974)
- Testing
- arthroscopic shoulder surgery of rotary cuff (ISB), arthroscopic shoulder surgery of rotary cuff (CSB)
- Volunteers
- 108 people
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche
Rotator Cuff Tear, Rotator Cuff Tear or Rupture, Not Specified as Traumatic
Shoulder Surgery Traditional vs Accelerated Rehabilitation Trial
This is a randomised controlled trial involving patients who have a double-row arthroscopic rotator cuff repair. Null hypothesis: There is no difference in outcome between standard rehabilitation and accelerated rehabilitation…
- Trial name
- S-START (NCT03913611)
- Testing
- Accelerated rehabilitation protocol, Traditional rehabilitation protocol
- Where
- United Kingdom
- Volunteers
- 50 people
- Sponsor
- Manchester University NHS Foundation Trust
Rotator Cuff Tear
Outcomes After Repair of Acute Rotator Cuff Tears
Few studies are considering acute traumatic rotator cuff tears in previously asymptomatic patients. The purpose of the current study was to investigate if delay of surgery, age at repair and the number of cuff tendons involved…
- Trial name
- HBStud2 (NCT01140230)
- Volunteers
- 42 people
- Sponsor
- University Hospital, Linkoeping
Rotator Cuff Injuries
A Pilot Randomized Trial of Pain Neuroscience Education in the Rehabilitation After Arthroscopic Rotator Cuff Repair
The aim of this study was to evaluate the effects of a 8-week pain neuroscience education programme compared to a biomedical education programme on the rehabilitation of patients who undergo arthroscopic rotator cuff repair.
- Trial name
- NCT04522934
- Testing
- Pain Neuroscience Education, Biomedical Education
- Where
- Chile
- Volunteers
- 29 people
- Sponsor
- Universidad Católica del Maule