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Bankart Lesion clinical trials

View clinical trials related to Bankart Lesion.

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NCT ID: NCT03693716 Completed - Clinical trials for Anterior Shoulder Dislocation

Dynamic Anterior Stabilization With Transsubscapular Long Head of the Biceps

Start date: September 20, 2018
Phase: N/A
Study type: Interventional

Clinical study of patients with a history of traumatic anterior shoulder dislocations to test the hypothesis that the arthroscopic dynamic anterior capsular stabilization technique with trans subscapular long head of the biceps tenodesis produces progressive good clinical and imagiological results.

NCT ID: NCT03594071 Completed - Clinical trials for Acetabular Labrum Tear

S&P of Q-Fix™ All-Suture Anchor System

Start date: August 31, 2018
Phase:
Study type: Observational

Post-market clinical follow-up needed to address existing clinical data and gaps on the existing Q-Fix™ device and meet existing MDD/MEDDEV requirements

NCT ID: NCT03525275 Completed - Pain, Postoperative Clinical Trials

Effect of Battlefield Acupuncture and Physical Therapy Versus Physical Therapy Alone After Shoulder Surgery

Start date: August 15, 2018
Phase: N/A
Study type: Interventional

The purpose of this randomized clinical trial is to determine the effectiveness of Battlefield Acupuncture (BFA) in addition to usual post-surgical shoulder physical therapy compared to a standard shoulder rehabilitation program in reducing medication use and pain in patients who have undergone shoulder surgery. Measurements of medication (opioid, NSAID, acetaminophen, etc.) use (daily number of pills consumed), pain rating, patient specific functional scale and global rating of change will be taken at 24, 72 hours, 7 days, 14 days and at six weeks post-surgery. It is hypothesized that the inclusion of Battlefield Acupuncture will result in a decrease in medication use and post-surgical pain when compared to rehabilitation alone. The population for this study is male and female DoD beneficiaries, ages 17-55 (17 if cadet) that are not participating in other shoulder research studies. The subjects in the experimental group will receive Battlefield Acupuncture in addition to their respective post-surgical shoulder rehabilitation protocol.

NCT ID: NCT03347019 Completed - Bankart Lesion Clinical Trials

Accelerated Rehabilitation After Arthroscopic Bankart Repair Surgery

Start date: December 15, 2016
Phase: N/A
Study type: Interventional

The aim of this study was to prospectively evaluate the efficacy of an accelerated rehabilitation regime for patients undergoing early arthroscopic stabilization for first-time anterior dislocation in terms of clinical outcome, return to play data and recurrence rates.

NCT ID: NCT03315819 Completed - Bankart Lesion Clinical Trials

Anterior Capsulo-labral Reinsertion by Arthroscopic Approach Versus Immobilization

BANKART
Start date: March 27, 2014
Phase: N/A
Study type: Interventional

The risk of recurrence and chronic instability after an initial episode of anterior glenohumeral dislocation is high, the risk is higher the younger the patient is. Most patients with recurrences develop this instability during the first 2 years. Several studies have shown that an initial arthroscopic surgical treatment (Bankart intervention) decreased the risk of recurrence and therefore of chronic instability, but this attitude is not usual in France and none randomized study comparing intervention of arthroscopic Bankart and immobilization was published by a French team. The primary objective was to evaluate at 2 years the efficacy on the rate of recurrent instability of the first-line arthroscopic repair of prior capsulo-labral lesions compared to conservative treatment by immobilization for patients under 25 years having an initial episode of anterior glenohumeral dislocation Material and method : We conducted a randomized controlled, open-label, parallel-group study (conservative treatment group by immobilizing VS surgical treatment group) in patients aged 18 to 25 with anterior glenohumeral primo luxation. Patients were clinically reassessed at 2 years with functional scores (WOSI, DuplayWalch, DASH), mobility and instability recurrence. Hypothesis: reduction of the recurrence rate in the surgically treated group