Clinical trials: Cuff
Rotator Cuff
Early Recovery After Surgery (ERAS)/Prehabilitation - Randomized Controlled Trial on the Implementation of ERAS/prehabilitation in Elective Reconstructive Shoulder Surgery
The aim of this randomized controlled trial is to investigate whether the intervention can improve the clinical outcome and patient satisfaction in elective reconstructive shoulder surgeries.
- Trial name
- Prehab (NCT06868472)
- Testing
- Prehabilitation, Control
- Where
- Germany
- Volunteers
- 84 people
- Sponsor
- Prof. Arasch Wafaisade
Intubation, Pain
The Cuff Pressure of an Endotracheal Tube After Supine-to-lateral Position Change
To compare the cuff pressure in lateral position between barrel-shaped cuff and taper-shaped cuff
- Conditions
- Intubation, Pain, Pharyngitis, Hoarseness
- Trial name
- LateralCuff (NCT02165319)
- Testing
- Barrel, Tapered
- Where
- South Korea
- Volunteers
- 58 people
- Sponsor
- Seoul National University Hospital
Orthopedic Disorder, Arthritis Shoulder
Blueprint® Mixed Reality Pilot Study
A pilot Single-Arm, Multicenter, Prospective, Post-Market 6 months Follow-Up Clinical Investigation to Evaluate the Safety and Effectiveness of the Blueprint Mixed Reality HOLOBLUEPRINT™ (HOLOBLUEPRINT™).
- Conditions
- Orthopedic Disorder, Arthritis Shoulder, Arthritis, Degenerative, Cuff Tear Arthropathy
- Trial name
- BLUEMR (NCT06080412)
- Where
- 4 sites in France
- Volunteers
- 44 people
- Sponsor
- Stryker Trauma and Extremities
Gynecologic Surgical Procedures
Barbed vs Standard Suture for Laparoscopic Vaginal Cuff Closure
Total laparoscopic hysterectomy is a procedure that is performed each time more often. One of the problems described for this procedure has to do with the closure of the vaginal vault, increased surgical time when suture…
- Trial name
- NCT03038945
- Testing
- 2/0 barbed suture, 0/0 Vicryl suture
- Where
- Colombia
- Volunteers
- 150 people
- Sponsor
- CES University
Rotator Cuff Syndrome
Comparative Effects of Spencer Techniques and Movement With Mobilization in Improving Pain, Range of Motion, and Functional Disability in Rotator Cuff Syndrome.
This study will be randomised clinical trial conducted at the University of Lahore Teaching Hospital, Lahore, Pakistan. A total of 60 participants will be selected and randomly allocated into two treatment groups (30 participants…
- Trial name
- NCT07458711
- Testing
- Spencer technique, Movement with mobilization, conventional physical therapy
- Where
- Pakistan
- Volunteers
- 60 people
- Sponsor
- University of Lahore
Rotator Cuff Injury
Comparison of Paracoracoid Subscapularis Plane Block to Interscalene Block for Arthroscopic Shoulder Surgery
One hundred and twenty patients will be randomized to Interscalene block or Paracoracoid Subscapularis plane block. The study will evaluate the efficacy and duration of blocks in the 2 groups with regards to postoperative…
- Trial name
- SPBvsISB (NCT03073928)
- Testing
- Interscalene Block, Paracoracoid SPB, Ropivacaine
- Where
- Canada
- Volunteers
- 120 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
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
Blood Pressure
Blood Pressure Monitor Clinical Test (Cuff Range: 22 Cm-42cm)
The purpose of this study is to monitor the blood pressure level of the patient using a preformed cuff ranged 22 cm-42 cm.
- Trial name
- NCT01575067
- Volunteers
- 85 people, healthy volunteers welcome
- Sponsor
- Andon Health Co., Ltd
Rotator Cuff Tear
Single Versus Double Row Suture Anchor Repair in Medium to Large Rotator Cuff Tears
The purpose of this study is to determine whether double row repair is better in healing than traditional single row repair in arthroscopic rotator cuff repair.
- Trial name
- NCT01039571
- Testing
- double row repair
- Where
- South Korea
- Volunteers
- 71 people
- Sponsor
- Samsung Medical Center
Tourniquets, Knee Arthroplasty, Total
Tourniquet Pressure in Primary Total Knee Arthroplasty
This proposed novel randomized control trial (RCT) seeks to address this gap in TKA protocol by gaining a better understanding of the relationship between tourniquet pressure and time, and intraoperative performance and…
- Conditions
- Tourniquets, Knee Arthroplasty, Total, Knee Replacement, Total
- Trial name
- NCT02830087
- Testing
- Tourniquet Cuff Pressure
- Where
- 2 sites in United States
- Volunteers
- 21 people, healthy volunteers welcome
- Sponsor
- Wake Forest University Health Sciences
Shoulder Impingement Syndrome
Comparison of Exercise Interventions in Adults With Subacromial Impingement Syndrome
The purpose of this study is to compare two different physical therapy exercise programs in persons who have shoulder pain in order to determine if they have a different affect on pain level and ability to use the injured…
- Trial name
- NCT01508715
- Testing
- Shoulder resistive exercise
- Where
- United States
- Volunteers
- 36 people
- Sponsor
- Texas Woman's University
Tendinopathy
Effect of Muscle Coactivation Strengthening for Rotator Cuff Tendinopathy
Rotator cuff tendinopathy (RCT) is the most frequent cause of shoulder pain. RCT is frequently termed as impingement syndrome, based on the underlying mechanism in which the subacromial space soft tissues (subacromial bursa…
- Trial name
- coacticuff (NCT02837848)
- Testing
- Coactivation Strengthening, Regular Strengthening
- Where
- Canada
- Volunteers
- 42 people
- Sponsor
- Université de Sherbrooke
Neuromuscular Blockade
Validation of the TOF Cuff Monitor® Which Measures Neuromuscular Block on the Upper Arm
Neuromuscular blocking agents (NMBAs) are frequently used in anesthesia and quantitative neuromuscular monitoring is standard care.
- Trial name
- NCT03256955
- Testing
- Tof cuff, Tof Watch SX
- Where
- Switzerland
- Volunteers
- 40 people
- Sponsor
- Christoph Czarnetzki
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.
Subacromial Decompression
Effects of Supervised Physical Therapy With Early Activation of the Rotator Cuff Versus Home Exercises in Patients After Arthroscopic Subacromial Decompression
The objective of this study was to evaluate and compare two different post-surgical rehabilitation strategies, Rehabilitation supervised by a physical therapist including exercises with progressive early activation of the rotator…
- Trial name
- NCT01054326
- Testing
- Exercises
- Volunteers
- 45 people
- Sponsor
- Linkoeping University
Intubation, Intratracheal
Transesophageal Echocardiography(TEE) Probe Insertion and Tracheal Cuff Pressure
Tracheal cuff overinflation is known to reduce tracheal mucosal blood flow and to increase tracheal morbidity. Transesophageal echocardiography (TEE) probe insertion may increase the tracheal cuff pressure.
- Trial name
- TEE (NCT02034643)
- Testing
- balloon pressure adjustment
- Where
- South Korea
- Volunteers
- 44 people
- Sponsor
- Seoul National University Hospital
Rotator Cuff Tear
Perioperative Polmacoxib Reduce Opioid Consumption for Post Operative Pain After Rotator Cuff Tear.
1. One day (±1 day) before surgery: The investigator or designated study staff will thoroughly explain the clinical trial process to the participant and their guardian (representative) based on the informed consent form and…
- Trial name
- NCT06590714
- Testing
- Experimental(Acelex cap m2mg), Active Comparator(NSAIDs-excluded non-opioid or opioid analgesics)
- Where
- South Korea
- Volunteers
- 150 people
- Sponsor
- Eulji University Hospital
Rotator Cuff Tear Arthropathy
Impact of Humeral Component Version on Outcomes Following RTSA
The proposed study is a prospective, single-blinded, randomized trial to investigate the impact of humeral component version on shoulder range of motion and patient reported functional outcomes following reverse total shoulder…
- Trial name
- NCT03111147
- Testing
- 0 degrees humeral component version, 30 degrees humeral component retroversion
- Where
- United States
- Volunteers
- 95 people
- Sponsor
- Corewell Health East
Rotator Cuff Tear
Effect of Dexmedetomidine on Postoperative Cognitive Function in Patients Undergoing Shoulder Arthroscopy With Beach Chair Position Under Desflurane Anesthesia
Investigate the effects of dexmedetomidine on postoperative cognitive function in patients undergoing shoulder arthroscopy with beach chair position under desflurane anesthesia.
- Trial name
- NCT02643017
- Testing
- Dexmedetomidine, normal saline
- Where
- South Korea
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Yonsei University
Tendinopathy
Effect of PRP vs Corticosteroid in Rotator Cuff Tendinopathy Subtypes in Arthroscopic Repair
Prospective, multicenter, randomized, single-blinded, parallel group，placebo-controlled，three-group establishment of specific treatment regimen for subtypes of tendinopathy
- Trial name
- NCT05603468
- Testing
- platelet rich plasma, Corticosteroid, Normal saline
- Where
- China
- Volunteers
- 387 people
- Sponsor
- Second Affiliated Hospital, Zhejiang University, School of Medicine