Clinical trials: Laceration Repair
Arthroscopic Surgical Treatment of High-grade (>50%) Partialthickness
Treatment of Partial-Thickness Rotator Cuff Tears
The goal of this clinical trial is to demonstrate that REGENETEN is superior to standard repair techniques when surgically treating high-grade (>50%) partial-thickness tears.
- Trial name
- REGEN PUB 2018 (NCT03734536)
- Testing
- REGENETEN™ Bioinductive Implant, Arthroscopic repair of the high-grade (>50%) partial-thickness
- Where
- 10 sites in United States
- Volunteers
- 168 people
- Sponsor
- Smith & Nephew, Inc.
Rotator Cuff Tears
Measuring Opioid Use After Rotator Cuff Repair: Comparing the Effects of Standard vs. Extended-release Nerve Blocks
The investigators aim to determine if a longer acting nerve block, which is a local anesthetic, can help reduce opioid use after surgery in patients that are getting rotator cuff repair surgery.
- Trial name
- NCT05482113
- Testing
- Liposomal bupivacaine, Bupivacaine Hcl 0.25% Inj
- Where
- United States
- Volunteers
- 17 people
- Sponsor
- Carilion Clinic
Meniscal Tear
Rehabilitation With or Without Knee Orthosis Following Meniscal Repair
RCT to determine if a less restrictive postoperative rehabilitation protocol following meniscal repair results in a faster return to normal knee function without compromising rates of healing.
- Trial name
- NCT05557916
- Testing
- Standard rehab, accelerated rehab group
- Where
- 2 sites in Sweden
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Karolinska Institutet
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 Syndrome, Rotator Cuff Injury
Allograft Reconstruction of Massive Rotator Cuff Tears vs Partial Repair Alone
The investigators hypothesize that the use of an allograft adjuvant to partial repair will lead to improved shoulder outcome measure scores compared to partial repair alone in massive rotator cuff tears.
- Conditions
- Rotator Cuff Syndrome, Rotator Cuff Injury, Disorder of Rotator Cuff, Full Thickness Rotator Cuff Tear
- Trial name
- NCT01987973
- Testing
- Partial Rotator Cuff Repair, Partial Rotator Cuff Repair with Allograft Augmentation
- Where
- Canada
- Volunteers
- 29 people
- Sponsor
- Ivan Wong
Laceration, Pain
The Addition of Oral Analgesics to LET During Laceration Repair
Background Approximately 30 million children are treated in emergency departments each year in the United States, of which two to three million are children presenting with lacerations.
- Trial name
- NCT01268670
- Testing
- Ibuprofen, Oxycodone
- Where
- United States
- Volunteers
- 150 people
- Sponsor
- Children's Hospitals and Clinics of Minnesota
Lacerations
A Randomized, Clinical Trial of Oral Midazolam Versus Oral Ketamine for Sedation During Laceration Repair.
Sedation is often needed for young children undergoing minor procedures in the emergency department (ED). Oral midazolam is one of the most commonly used regimens for children undergoing laceration repair but its sedative…
- Trial name
- NCT01925898
- Testing
- Midazolam - active comparator, Experimental Arm: Ketamine
- Where
- Israel
- Volunteers
- 60 people
- Sponsor
- Assaf-Harofeh Medical Center
Bone Marrow Stimulating, Modified Suture Bridge
Prospective Randomized Controled Study on the Outcome of Greenhouse Tec in the Arthroscopic Treatment of Small to Medium Rotator Cuff Tear
This study is aprospective cohort study on the outcome of a combination of bone marrow stimulation and modified suture bridge in the arthroscopic treatment of small and medium rotator cuff tear.
- Trial name
- NCT04695626
- Testing
- The combination of bone marrow stimulation and modified suture bridge(Greenhouse tec)
- Where
- China
- Volunteers
- 72 people
- Sponsor
- Beijing Jishuitan Hospital
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
Children Requiring Sedation to Facilitate Laceration Repair
Volumes of Administration for Intranasal Midazolam
The purpose of this study is to determine exactly how much drug volume should be administered into each nare, so that the drug absorption can be maximized and the amount that runs out of the nose, or is swallowed, is minimized…
- Trial name
- NCT01948908
- Testing
- Intranasal midazolam
- Where
- United States
- Volunteers
- 99 people
- Sponsor
- Columbia University
Lacerations, Wounds
Evaluation of microMend Device to Close Lacerations
In this study, total of 20 subjects will have lacerations will be closed with microMend, which is an FDA-listed wound closure product.
- Trial name
- NCT03830515
- Testing
- microMend
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- KitoTech Medical, Inc.
Rupture of Hip Abductor Tendon (Disorder)
Hip Abductor Tendon Repair Versus Sham Surgery
This study will examine the effectiveness of open surgical reconstruction in the treatment of patients with hip abductor tendon tears.
- Trial name
- NCT06398015
- Testing
- Surgical reconstruction of hip abductor tendon tear
- Where
- Denmark
- Sponsor
- Horsens Hospital
Rotator Cuff Tear
Effect of Postoperative Immobilization on Healing After Rotator Cuff Arthroscopic Repair
The study aims to establish whether one month postoperative immobilization compared early passive motion after rotator cuff arthroscopic repair in small or medium ruptures with double row technique has any healing significance.
- Trial name
- NCT01502098
- Testing
- Postoperative early passive motion, Sling
- Where
- Argentina
- Volunteers
- 114 people
- Sponsor
- Hospital Italiano de Buenos Aires
CerebroSpinal Fluid (CSF) Leak, Dural Tear
A Prospective, Randomized, Two-Arm, Controlled, Single-Blind, Multi-Center Study to Evaluate the Safety and Efficacy of ArtiFix® Dural Repair Sealant Graft in Cranial and Spine Surgery (NEOFIX Study)
The purpose of the NEOFIX study is to evaluate the safety and efficacy of ArtiFix® dural sealant graft in comparison to usual treatment for Dural repair (membrane that covers the brain and spinal cord) following cranial and spine…
- Trial name
- NEOFIX (NCT07765862)
- Testing
- ArtiFix® is a surgical dural sealant graft intended to close dural defects following cranial and spine surgeries., Standard of Care (Investigator Choice)
- Volunteers
- 228 people
- Sponsor
- Nurami Medical Ltd
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
Rotator Cuff Tear
Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation
Prospective, randomized, multi-center, controlled study for patients undergoing open rotator cuff repair. Patients are stratified based on tear size to one of three groups.
- Trial name
- NCT00957255
- Testing
- OrthoADAPT, Standard of care
- Where
- United States
- Sponsor
- Baxter Healthcare Corporation
Meniscus Tear
SoftStitch™ for All-Inside Meniscal Repair: Comparative Analysis of Patient Reported Outcome Measures
Acute and traumatic knee meniscus tears are a frequent occurrence. Evidence shows meniscal repair results in more favorable patient reported outcomes and articular cartilage preservation.1 This prospective, multicenter, single…
- Trial name
- NCT05491564
- Testing
- SoftStitch™
- Volunteers
- 50 people
- Sponsor
- Arthrex, Inc.
Rotator Cuff Tear
The Impact of Psychological Factors on the Outcome of Surgical Repair for Rotator Cuff
The proposed study will be a multi-centre, prospective, observational cohort to determine if psychological well-being has an impact on the outcome of surgical repair for rotator cuff tears.
- Trial name
- IMPROVE (NCT03018210)
- Testing
- Surgical repair of the rotator cuff
- Where
- 5 sites in Canada
- Volunteers
- 267 people
- Sponsor
- Unity Health Toronto
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, Shoulder Surgery
Interscalene Brachial Plexus Block and Early Wound-Related Symptoms After Open Rotator Cuff Repair
This exploratory randomized controlled trial evaluated the association of interscalene brachial plexus block (ISB) with early postoperative wound-related symptom scores and perioperative biomarker responses in patients undergoing…
- Conditions
- Rotator Cuff Tear, Shoulder Surgery, Postoperative Recovery
- Trial name
- NCT05499897
- Testing
- Ultrasound-Guided Interscalene Brachial Plexus Block, General Anesthesia
- Where
- Turkey (Türkiye)
- Volunteers
- 34 people
- Sponsor
- Yuzuncu Yil University