Clinical trials: Laceration Repair
Rotator Cuff Tear
BioWick SureLock Clinical Outcomes Study
The purpose of this study is to collect postmarket data in subjects who receive surgical treatment of a full-thickness rotator cuff tear (of at least 1.5 cm) with the BioWick™ SureLock™ implant.
- Trial name
- NCT03199391
- Testing
- BioWick SureLock Implant
- Where
- 7 sites in United States
- Volunteers
- 71 people
- Sponsor
- Zimmer Biomet
Proximal Humeral Fracture Fixated With PHILOS© Plate, Rotator Cuff Tear Surgical Repair
Dry Needling in Post-operative Shoulder Pain
Fractures of the proximal humerus account for between 5% and 8% off all reported fractures. Post-operative shoulder pain is highly frequent.
- Trial name
- NCT02122315
- Testing
- Physical therapy plus dry needling, Physical therapy
- Where
- Spain
- Volunteers
- 20 people
- Sponsor
- César Fernández-de-las-Peñas
Meniscus Tear, Retention; Meniscus
Circumferential Compression STITCH Repairs of Complex and Horizontal Cleavage Meniscal Tears
The purpose of this study is to understand the benefits and safety of the NOVOSTITCH PRO Meniscal Repair (NOVOSTITCH PRO) system. The meniscus is a tissue in the knee joint.
- Trial name
- NOVOSTITCH PRO (NCT04361487)
- Testing
- NOVOSTITCH™ PRO Meniscal Repair System
- Where
- 6 sites in United States
- Volunteers
- 33 people
- Sponsor
- Smith & Nephew, Inc.
Rotator Cuff Tear Arthropathy, Repair of a Cuff Tear
Efficacy and Safety of Digital Therapeutics for Improving Shoulder Function After Rotator Cuff Repair
1. Importance of Rehabilitation After Rotator Cuff Repair Rotator cuff tears are among the most common shoulder conditions in Korea. They can occur naturally with aging or result from trauma or overuse.
- Trial name
- NCT07255534
- Testing
- digital therapeutics, usual care
- Where
- South Korea
- Volunteers
- 70 people
- Sponsor
- Samsung Medical Center
Rotator Cuff Tears, Rotator Cuff Tear Arthropathy
From Rotator Cuff Repair to Reverse Shoulder Arthroplasty - Clinical and Radiological Results
In the planned study the investigators will invite 733 participants 10 years after arthroscopic rotator cuff repair to a follow up examination. Shoulder pain is a common problem in the Norwegian population.
- Conditions
- Rotator Cuff Tears, Rotator Cuff Tear Arthropathy, Rotator Cuff Injuries
- Trial name
- NCT06644729
- Testing
- Arthroscopic Rotator Cuff Repair
- Where
- Norway
- Volunteers
- 733 people
- Sponsor
- Lovisenberg Diakonale Hospital
Acetabular Labrum Tear
The Arthroscopic Labral Excision or Repair Trial (ALERT)
This study compares two established surgical treatments for acetabular labral tears. Patients will be prospectively recruited and randomised to either labral repair or debridement.
- Trial name
- ALERT (NCT03257709)
- Testing
- Arthroscopic acetabular labral repair, Arthroscopic acetabular labral resection
- Where
- United Kingdom
- Volunteers
- 96 people
- Sponsor
- University of Oxford
Meniscal Tear
Meniscal Repair: A Randomized Prospective Trial of FAST-FIX vs. Meniscal Suturing
Meniscal repair resulting in meniscal preservation is the most desirable treatment of a torn meniscus and is one of the most commonly performed arthroscopic procedures.
- Trial name
- NCT00284661
- Testing
- FAST FIX, Meniscal suturing
- Where
- Canada
- Volunteers
- 132 people
- Sponsor
- Fowler Kennedy Sport Medicine Clinic
Rotator Cuff Tear Repair Anchors
Evaluation of the Healicoil Suture Anchor for Rotator Cuff Repair
The purpose of the proposed study is to evaluate a new anchor for rotator cuff repair, the Smith \& Nephew Healicoil anchor. This anchor utilizes a small open-construct design to promote bone-in growth and potentially allow for…
- Trial name
- NCT02759458
- Testing
- Smith & Nephew Healicoil Anchor, Smith & Nephew Twinfix Anchor
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Rush University Medical Center
Laceration of Skin
Evaluation of Zip Device to Conventional Sutures for Laceration Repair in Pediatrics in an Emergency Department
A prospective, randomized, controlled post-market clinical investigation that will enroll pediatric subjects requiring laceration repair.
- Trial name
- ZIPPED (NCT04122859)
- Testing
- Zip Skin Closure Device
- Where
- Israel
- Volunteers
- 30 people
- Sponsor
- ZipLine Medical Inc.
Rotator Cuff Tear
Prospective Sensor Controlled Compliance Analysis of Shoulder Abduction Splint After Rotator Cuff Repair
The postoperative shoulder rehabilitation in an abduction brace after rotator cuff reconstruction of the shoulder is crucial for a successful healing of the reconstruction.
- Trial name
- SENSABDUKT (NCT03054753)
- Testing
- Abduction brace wearing time analysis
- Where
- Switzerland
- Volunteers
- 46 people, healthy volunteers welcome
- Sponsor
- Balgrist University Hospital
Rotator Cuff Tears
Long-Term Follow-up of Arthroscopic Biceps Tenotomy and Subacromial Decompression in Chronic Massive Rotator Cuff Tears
Chronic massive rotator cuff tears (MMRCTs) are a significant orthopedic challenge, often leading to significant shoulder pain and functional impairment.
- Trial name
- NCT06743061
- Testing
- Post-Op Follow Up
- Where
- Egypt
- Volunteers
- 23 people
- Sponsor
- Cairo University
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
Rotator Cuff Tears, Rotator Cuff Injuries
Comparison of Two Arthroscopic Rotator Cuff Repair Techniques: Knot-tying Versus Knotless Suture-bridge Technique
Suture-bridge technique has been widely used for rotator cuff tears with many studies showing superior clinical results and lower failure rates compared to other techniques.
- Trial name
- NCT03982108
- Testing
- Arthroscopic rotator cuff repair with knotless suture-bridge technique, Arthroscopic rotator cuff repair with knot-tying suture-bridge technique
- Where
- Turkey (Türkiye)
- Volunteers
- 104 people
- Sponsor
- Koray Sahin
Rotator Cuff Tear
Superior Capsular Reconstruction vs. Partial Repair for Massive Rotator Cuff Tears
Little evidence exists to guide treatment in patients with massive irreparable rotator cuff tears (MRCTS). Arthroscopic partial rotator cuff repair (PRCR) has the longest record of use.
- Trial name
- SCR (NCT03617562)
- Testing
- Superior Capsular Reconstruction, Partial Repair
- Where
- 2 sites in Canada
- Volunteers
- 70 people
- Sponsor
- Sunnybrook Health Sciences Centre
Rotator Cuff Tear
Effectiveness of the Ivivi Torino II, Pulsed Radio Frequency Device, on Narcotic Use, Pain and Quality of Life Following Shoulder Arthroscopic Rotator Cuff Repair.
To determine the effectiveness of non-thermal PRF delivered with the Ivivi Torino II on narcotic use, pain, and health-related quality of life following shoulder arthroscopic rotator cuff surgery comparing: Active treatment…
- Trial name
- NCT01507818
- Testing
- Ivivi Torino II
- Where
- 3 sites in United States
- Volunteers
- 37 people
- Sponsor
- Amp Orthopedics, Inc.
Femoroacetabular Impingement Syndrome, Acetabular Labral Tear
Postoperative Hip Bracing After Hip Arthroscopy
Hip arthroscopy for treatment of femoroacetabular impingement syndrome (FAIS) involves reshaping of the osseous sources of impingement ("osteoplasty") and treatment of impingement-associated labral tears with labral repair.
- Trial name
- NCT04599296
- Testing
- Hip brace
- Where
- United States
- Volunteers
- 82 people
- Sponsor
- University of Washington
Meniscus Tear
The Effect of Centralization on Medial Meniscal Extrusion for Medial Meniscus Posterior Root Tear Repair
The purpose of this research is to determine if meniscus root repair with or without centralization will have an impact on postoperative pain, function, activity levels, patient satisfaction, and incidence of revision meniscus…
- Trial name
- NCT07388290
- Testing
- Medial meniscus posterior root tear (MMPRT) repair with meniscus centralization, Medial meniscus posterior root tear (MMPRT) repair without meniscus centralization
- Where
- 3 sites in United States
- Volunteers
- 54 people
- Sponsor
- Mayo Clinic
Meniscus Tear Caused by a Traumatic Event, Fibrin Clot Augmentation
A Comparative Prospective Study of the Arthroscopic Meniscal Repair Methods
Performing arthroscopic meniscus repair following a traumatic meniscus tear as an alternative to a meniscectomy is now an acceptable choice.
- Conditions
- Meniscus Tear Caused by a Traumatic Event, Fibrin Clot Augmentation, Meniscal Repair
- Trial name
- NCT06176183
- Testing
- Arthroscopic meniscus repair
- Where
- 2 sites in Lithuania
- Volunteers
- 100 people
- Sponsor
- Vilnius University
Femoro Acetabular Impingement, Pain, Postoperative
Outcomes of CPM Usage Following Arthroscopic Acetabular Labral Repair
The purpose of this study is to measure whether CPM (continuous passive motion) usage improves outcomes following arthroscopic hip surgery that includes labral repair.
- Conditions
- Femoro Acetabular Impingement, Pain, Postoperative, Hip Labral Tear
- Trial name
- NCT03407612
- Testing
- Continuous Passive Motion
- Where
- United States
- Volunteers
- 54 people
- Sponsor
- Ohio State University
Knee Meniscus Tear
A Prospective, Post-market, Multi-center Feasibility Study of the BioDuct® Meniscal Repair Device
To demonstrate repair of the meniscus at 6 months, as evaluated by MRI, will be observed; and clinical qualitative assessments will improve from preoperative to postoperative time points with the BioDuct® Meniscal Repair Device.
- Trial name
- NCT01270919
- Testing
- BioDuct Meniscal Repair Device
- Where
- 3 sites in United States
- Volunteers
- 1 people
- Sponsor
- Stryker Orthopaedics