Clinical trials: Laceration Repair
Laceration
A Randomized Post-market Study to Evaluate Zip Device Compared to Sutures for Laceration Repair in Pediatrics and Adults
The Zip-009 clinical investigation will enroll 26 paediatric and adult subjects requiring laceration repair and fulfilling the eligibility criteria for the clinical investigation.
- Trial name
- NCT03199456
- Testing
- Zip surgical skin closure device, Standard of Care sutures
- Where
- 2 sites in Sweden
- Volunteers
- 26 people
- Sponsor
- ZipLine Medical Inc.
Rotator Cuff Tear, Rotator Cuff Repair of the Shoulder
The Contribution of Platelet-Rich Plasma to the Surgical Treatment of Rotator Cuff Tear: An Experimental Study
Purpose of the study: The aim of the study is to determine whether the postoperative administration of biological therapy with autologous platelet-rich plasma improves the clinical, imaging, and biochemical outcomes following…
- Conditions
- Rotator Cuff Tear, Rotator Cuff Repair of the Shoulder, PRP Injection
- Trial name
- NCT07689383
- Testing
- Arthroscopic repair of shoulder rotator cuff tear, PRP injection
- Where
- Greece
- Volunteers
- 51 people
- Sponsor
- KAT General Hospital
Rotator Cuff Tear
Use of Graft Jacket for Rotator Cuff Repair
This study is to evaluate the safety and effectiveness of GraftJacket, a human tissue product used in fixing large and massive reparable rotator cuff tears.GraftJacket allograft (Wright Medical Technology, Inc., Arlington, TN) is…
- Trial name
- NCT00456781
- Testing
- Augmentation, Rotator Cuff Repair without augmentation
- Where
- 7 sites in United States, Canada
- Volunteers
- 79 people, healthy volunteers welcome
- Sponsor
- Stryker Trauma and Extremities
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.
Rotator Cuff Tear, Postoperative Pain
Oral Ketorolac for Arthroscopic Rotator Cuff Repair
1. The investigators aim to examine the use of IV and oral ketorolac as an adjunctive agent to the standard of care pain protocol for postoperative pain control following arthroscopic rotator cuff repair. 2.
- Trial name
- NCT03967847
- Testing
- Ketorolac
- Where
- United States
- Volunteers
- 44 people
- Sponsor
- University Hospitals Cleveland Medical Center
Rotator Cuff Tear
Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair
Rotator cuff (RC) repair is one of the most common treatment approch to relief the pain and improve the shoulder function on patients with rotator cuff rupture.
- Trial name
- NCT03533088
- Testing
- Hospitalized rehabilitation, Home-based rehabilitation
- Where
- Turkey (Türkiye)
- Volunteers
- 54 people, healthy volunteers welcome
- Sponsor
- Hacettepe University
Rotator Cuff Injuries, Rotator Cuff Repair Rehabilition
Efficacy of Adding Early Scapular Muscles Strengthening Exercise After Rotator Cuff Repair on Scapula Kinematics
The study investigates the effect of accelerate rehabilitation protocol(adding scapular strengthen exercises (lower trapezius and serratus anterior) from week 1) after arthroscopic rotator cuff repair on scapular upward rotation…
- Conditions
- Rotator Cuff Injuries, Rotator Cuff Repair Rehabilition, Supraspinatus Tear
- Trial name
- NCT06851650
- Testing
- Rehabilition protocol after rotator cuff repair surgery
- Where
- 2 sites in Egypt
- Volunteers
- 30 people
- Sponsor
- Cairo University
Needlestick Injuries
Blunt Needles do Not Reduce Needlestick Injuries to Doctors During Suturing After Child-Birth
The hypothesis for this study is that use of blunt tipped needles used during the repair of an episiotomy (tear in the vagina after childbirth) will result in fewer needlestick injuries to the surgeon.
- Trial name
- NCT00536289
- Testing
- Blunt needle
- Where
- United States
- Volunteers
- 438 people, healthy volunteers welcome
- Sponsor
- Medical University of South Carolina
Procedural Anxiety
Dose-Finding Study of Intranasal Midazolam for Procedural Sedation in Children
Dose-finding study to compare intranasal midazolam doses of 0.2, 0.3, 0.4 and 0.5 mg/kg in children undergoing laceration repair to achieve the following aims: Specific Aim #1: To determine the most effective dose of intranasal…
- Trial name
- NCT04586504
- Testing
- Intranasal midazolam
- Where
- United States
- Volunteers
- 101 people
- Sponsor
- Columbia University
Rotator Cuff Tear or Rupture, Not Specified as Traumatic
Psychosocial Factors, Lifestyle and Central Pain Processing as Potential Predictors of Outcome for Rotator Cuff Repair
The influence of modifiable psychosocial and lifestyle factors and the role of central pain processing (CPP) on outcome after rotator cuff repair (RCR) is not well enough established to formulate holistic prognosis.
- Trial name
- NCT04946149
- Where
- Switzerland
- Volunteers
- 142 people
- Sponsor
- Kantonsspital Winterthur KSW
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
Arm Injuries
Pilot Study to Evaluate the Restore Orthobiologic Implant in Rotator Cuff Tear Repair
Primary Endpoints: Comparative evaluation of any differences between the two groups in change from baseline to the 3-month time point in terms of: Functional recovery (patient-based) - using the Oxford Shoulder Score.
- Trial name
- NCT00208338
- Testing
- RESTORE SIS Patch, Rotator cuff repair
- Where
- 2 sites in Belgium, United Kingdom
- Volunteers
- 33 people
- Sponsor
- DePuy International
Laceration Repair
Intranasal Dexmedetomidine Dose-finding Study
The most common injury prompting an emergency department (ED) visit in children is a cut (laceration) that requires repair using stitches or skin glue.
- Trial name
- NCT03957304
- Testing
- Dexmedetomidine
- Where
- Canada
- Volunteers
- 55 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Rotator Cuff Tear
A Selective COX-2 Inhibitor Provides Pain Control But Hinders Healing Following Arthroscopic Rotator Cuff Repair
Selective cyclooxygenase (COX)-2 inhibitors are commonly used analgesics that provide similar analgesia but reduced adverse effects compared to other analgesics.
- Trial name
- NCT02850211
- Testing
- Celecoxib, Ibuprofen, Tramadol
- Volunteers
- 180 people, healthy volunteers welcome
- Sponsor
- Seoul National University Bundang Hospital
Meniscus Tear
Novel Bioactive Sleeve on Pain and PROMs
A novel bioactive sleeve will be compared to a placebo sleeve with a similar look and feel to assess pain outcomes, patient reported outcome measures, and effectiveness of healing based on range of motion.
- Trial name
- NCT06041321
- Testing
- Reparel Sleeve
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Northwell Health
Rotator Cuff Tear
Surgical Safety and Effectiveness in Orthopedics: Swiss-wide Multicenter Evaluation and Prediction of Core Outcomes in Arthroscopic Rotator Cuff Reconstruction
Surgical safety and effectiveness in orthopedics: Swiss-wide multicenter evaluation and prediction of core outcomes in arthroscopic rotator cuff reconstruction.
- Trial name
- ARCR_Pred (NCT04321005)
- Testing
- arthroscopic rotator cuff reconstruction
- Where
- 20 sites in Germany, Switzerland
- Volunteers
- 973 people
- Sponsor
- University Hospital, Basel, Switzerland
Facial Lacerations
Cosmetic Outcomes and Patient Satisfaction After Facial Laceration Repair in the Emergency Department
Facial lacerations are commonly treated in the emergency department. The nature of the injury leads to a great deal of concern about the long-term cosmetic appearance of the wounds. Research Questions 1.
- Trial name
- NCT01514084
- Where
- United States
- Volunteers
- 160 people
- Sponsor
- Children's Hospitals and Clinics of Minnesota
Rotator Cuff Tear
Preoperative Central Sensitization and Postoperative Outcomes After Arthroscopic Rotator Cuff Repair
This prospective observational study aims to investigate the effect of preoperative central sensitization on postoperative clinical outcomes in patients undergoing arthroscopic rotator cuff repair.
- Trial name
- ARCS (NCT07667257)
- Testing
- Arthroscopic Rotator Cuff Repair
- Volunteers
- 50 people
- Sponsor
- Medipol University
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
Supraspinatus Tear
Does Autologous Conditioned Plasma Enhance Rotator Cuff Tendon Healing After Surgery?
The aim of this study is to establish if the application of autologous conditioned plasma (ACP), also described as platelet rich plasma (PRP), to the site of supraspinatus tendon repair beginning within two weeks of surgery, can…
- Trial name
- NCT01414764
- Testing
- Autologous conditioned plasma (ACP)
- Where
- Australia
- Volunteers
- 60 people
- Sponsor
- The University of Western Australia