Clinical trials: Laceration Repair
Meniscal Injuries
Novel One-step Repair of Knee Meniscal Tear Using Platelet-rich Fibrin
Currently, most knee meniscal tears are treated by partial or complete meniscectomy, or by suture repair when it is possible. Recently, the investigators have successfully developed and implanted a novel biomaterial…
- Trial name
- NCT01211119
- Testing
- No PRF
- Where
- Taiwan
- Volunteers
- 18 people
- Sponsor
- Taipei Medical University WanFang Hospital
Rotator Cuff Tear, Muscle Atrophy
Stromal Vascular Fraction Cell Therapy to Improve the Repair of Rotator Cuff Tears
Rotator cuff disease is one of the most prevalent musculoskeletal conditions across the world. Patients with chronic rotator cuff tears often have substantial muscle atrophy and fatty infiltration.
- Conditions
- Rotator Cuff Tear, Muscle Atrophy, Tendon Tear
- Trial name
- NCT03332238
- Testing
- Autologous Stomal Vascular Fraction Material, Ringer's solution
- Where
- United States
- Volunteers
- 56 people
- Sponsor
- Hospital for Special Surgery, New York
Meniscus Tear, Meniscus; Derangement
Enhancing Recovery Through a Combined Mechanobiologic Intervention Following Meniscus Repair
Arthroscopic meniscal procedures are the most commonly performed orthopaedic procedure in the U.S. affecting 15% of Americans ages 10-65 years.
- Conditions
- Meniscus Tear, Meniscus; Derangement, Meniscus Lesion, Meniscus Disorder
- Trial name
- NCT05505747
- Testing
- Fisetin
- Where
- United States
- Sponsor
- Austin V Stone
Glenoid Labrum Tear
Blood Flow Restriction Training Following Glenoid Labral Repair
The objective of this study is to evaluate the effects of BFR training on patient reported outcome measures and shoulder muscle girth in patients following glenoid labral repair.
- Trial name
- NCT03675620
- Testing
- BFR, Standard Rehabilitation
- Where
- United States
- Sponsor
- Andrews Research & Education Foundation
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
Did MRI Appearance of Supraspinatus Muscle Atrophy Changes After Repair of All Kind of Rotator Cuff Tear?
There are two purpose of this study, first is to find whether arthroscopic rotator cuff repair is changing the appearance of supraspinatus muscle atrophy in each and every patient.
- Trial name
- NCT02628457
- Testing
- arthroscopic rotator cuff repair
- Where
- South Korea
- Volunteers
- 209 people
- Sponsor
- CM Chungmu Hospital
LET, Laceration of Skin
Comparison of 2 Application Techniques for LET Gel Used Prior to Simple Laceration Repair
To compare pain scores during laceration repair with first suture placement using standardized visual analog scale (VAS) between 2 different topical local anesthetic application techniques for using LET gel.
- Trial name
- LET (NCT04536493)
- Testing
- LET (lidocaine 4%; epinephrine 0.1%; tetracaine 0.5%) gel (1 application), LET (lidocaine 4%; epinephrine 0.1%; tetracaine 0.5%) gel (3 applications)
- Where
- United States
- Volunteers
- 48 people
- Sponsor
- Children's Hospital of Orange County
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 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
Laceration
Intranasal Ketamine for Procedural Sedation in Pediatric Laceration Repair
The purpose of this study is to compare how well three different doses of ketamine, given as a spray into the nose, help to sedate children and help them tolerate repairs of cuts on their faces.
- Trial name
- NCT00451724
- Testing
- Intranasal ketamine
- Where
- United States
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- Rhode Island Hospital
Surgical Scar Tissue of Cesarean Section or Vaginal Tear or Episiotomy
Low Level Laser Therapy for Better Wound Healing
Prospective randomized double blind study. Intervention 1: Low-level laser therapy ca. 72 Joules vs. Intervention 2: No Low-level laser therapy. Outcome: Pain score \& would healing at discharge, 1 months \& 3 months
- Trial name
- NCT06220786
- Testing
- Low-level laser therapy, "Fake" low-level laser therapy
- Where
- Germany
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- St. Elisabethen Krankenhaus Frankfurt GmbH
Rotator Cuff Tear
Comparing the Outcomes Between Rotator Cuff Repair With and Without Suprascapular Nerve Decompression
The purpose of the study is to compare the differences in outcome between the traditional rotator cuff repair surgery and rotator cuff repair with suprascapular nerve decompression surgery.
- Trial name
- NCT02107573
- Testing
- Rotator Cuff Repair without Suprascapular Nerve decompression, Rotator Cuff Repair with Suprascapular Nerve decompression
- Where
- 2 sites in United States
- Volunteers
- 36 people
- Sponsor
- University of Chicago
Rotator Cuff Tear
Duration of Immobilization After Rotator Cuff Repair: Its Clinical Impact
The purpose of this study is to determine whether the immobilization period is helpful for the better healing of repaired rotator cuff.
- Trial name
- NCT00891566
- Testing
- Immobilization
- Where
- South Korea
- Volunteers
- 100 people
- Sponsor
- Samsung Medical Center
Unilateral Meniscus Tear of the Knee Joint
IIT Study on the Use of Medical Bio Glue for Repairing Meniscus Tears
To evaluate the safety and effectiveness of water triggered medical bioadhesive for meniscus tear repair
- Trial name
- NCT06878794
- Testing
- Using medical biological glue for filling And Using the meniscus suture system, Using the meniscus suture system
- Where
- China
- Volunteers
- 60 people
- Sponsor
- First Affiliated Hospital of Ningbo University
Rotator Cuff Tear Repair
TASK-ORIENTED REHABILITATION AFTER ROTATOR CUFF SURGERY
Rotator cuff tears negatively affect shoulder stability, range of motion, and performance in daily activities. Postoperative rehabilitation is essential for improving functional recovery and quality of life; however, conventional…
- Trial name
- NCT07665541
- Testing
- Task-oriented rehabilitation, Conventional rehabilitation group
- Where
- Turkey (Türkiye)
- Volunteers
- 14 people
- Sponsor
- Medipol University
Rotator Cuff Tear
Does the Suture-spanning Augmentation of Single-row Repair in Massive Rotator Cuff Tear Reduce the Retear Rate?
There are several associated structural changes when dealing with massive rotator cuff repair, which include tendon retraction and fragility, muscle atrophy and fatty infiltration, as well as osteoporosis over the tendon…
- Trial name
- NCT03609164
- Testing
- Suture-bridge augmentation of single-row repair
- Where
- Taiwan
- Volunteers
- 80 people
- Sponsor
- Taipei Veterans General Hospital, Taiwan
Meniscus Tear
Study to Evaluate the Safety and Efficacy of AM3101 to Augment Meniscal Healing
The purpose of this clinical trial is to assess the safety and efficacy of AM3101 to facilitate meniscal repair and reduce the incidence of non-healing complications and morbidities associated with a failed meniscal repair.
- Trial name
- NCT05560477
- Testing
- AM3101
- Where
- 3 sites in United States
- Volunteers
- 22 people
- Sponsor
- University of Cincinnati
Cerebrospinal Fluid Leak, Dural Tear
Safety and Efficacy Evaluation of ArtiFix® Sealant Graft in Subjects Requiring Dural Repair Following Neurosurgery
The purpose of this clinical study is to evaluate and establish the safety and efficacy of the ArtiFix® device in subjects scheduled for cranial or spinal surgery that requires Dural repair (membrane that covers the brain and…
- Trial name
- NCT07092267
- Testing
- ArtiFix® is a surgical dural sealant graft intended to close dural defects following cranial and spine surgeries.
- Volunteers
- 20 people
- Sponsor
- Nurami Medical Ltd
Meniscal Tear, Meniscus Tear
Study of Suture Repair of Torn Meniscus in the Knee
Horizontal meniscus tears meeting specified criteria will be repaired by any commonly used suture technique. Subjects will be followed for 2 years to evaluate the effectiveness of the repair, by assessing the re-operation rate…
- Trial name
- STITCH (NCT02237001)
- Testing
- Suture-based meniscal repair
- Where
- 8 sites in United States
- Volunteers
- 30 people
- Sponsor
- Smith & Nephew, Inc.
Rotator Cuff Tear, Rotator Cuff Tears
Post-Market Clinical Follow-up (PMCF) Study of the Pitch-Patch for the Augmentation or Reinforcement of the Rotator Cuff
This is a clinical investigation study. It will verify the long-term safety and performance of the Pitch-Patch when implanted to reinforce partially repairable rotator cuff tears and used as described by the manufacturer's…
- Conditions
- Rotator Cuff Tear, Rotator Cuff Tears, Rotator Cuff Tears of the Shoulder, Rotator Cuff Injuries
- Trial name
- NCT05906004
- Testing
- Pitch-Patch
- Where
- United Kingdom
- Volunteers
- 37 people
- Sponsor
- Xiros Ltd