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Anterior Shoulder Instability clinical trials

View clinical trials related to Anterior Shoulder Instability.

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NCT ID: NCT06154460 Not yet recruiting - Surgery Clinical Trials

The Effects of Different Surgical Stabilization Methods in Recurrent Anterior Shoulder Instability

SSM-SI
Start date: December 18, 2023
Phase:
Study type: Observational

Shoulder instability is the inability to retain the humeral head in the glenoid fossa. The incidence of instability is 8.2 to 23.9 per 100,000 person-years with an estimated prevalence of 1.7%. The most common shoulder instability with a rate of 98% is anterior dislocation, in which the humeral head is displaced anterior to the glenoid. Conservative and surgical treatments of instability are available. There are many controversial issues related to these methods in the literature. For example; an atrophy and functional loss in the infraspinatus after reimplissage, atrophy and loss of proprioception in the muscles around the shoulder after capsular repair, and loss of proprioception after the laterjet procedure have been reported.Therefore, the aim of this study was to compare different surgical stabilization methods in terms of pain, proprioceptive sensation, functional status and muscle activation in recurrent anterior shoulder instability, which is very common in adults.

NCT ID: NCT05431114 Recruiting - Clinical trials for Shoulder Dislocation

Quantitative MRI of Glenohumeral Cartilage & Labrum in Shoulder Instability

OREF
Start date: August 2, 2022
Phase:
Study type: Observational

The purpose of this study is to assess cartilage strain and contact areas following glenohumeral instability compared to healthy individuals.

NCT ID: NCT05151965 Recruiting - Clinical trials for Anterior Shoulder Dislocation

Return to Sport and Functional Performance Following Surgical Intervention for Anterior Glenohumeral Instability

Start date: September 1, 2022
Phase:
Study type: Observational

The purpose of this prospective cohort study is to compare patient-reported, clinical, and functional outcomes in patients who have elected to have either the Bankart with Remplissage or Latarjet procedure for the treatment of anterior glenohumeral instability (AGHI) up to 24-months postoperative.

NCT ID: NCT03985839 Active, not recruiting - Rotator Cuff Tears Clinical Trials

Safety and Performance of MICRORAPTORâ„¢ Suture Anchors in Shoulder and Hip

Start date: August 1, 2019
Phase:
Study type: Observational

This is a prospective, multi-center, PMCF study to evaluate the safety and performance of the MICRORAPTOR REGENESORB suture anchors, MICRORAPTOR Knotless REGENESORB suture anchors, and MICRORAPTOR Knotless PEEK suture anchors implanted in 300 subjects needing reattachment of soft tissue to bone.

NCT ID: NCT03458468 Completed - Clinical trials for Anterior Shoulder Instability

Tranexamic Acid for the Latarjet Procedure.

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The investigators propose a double-blinded randomized study evaluating the effectiveness of tranexamic acid in reducing postoperative swelling and haematoma formation after the Latarjet procedure. The purpose of this study is to assess the efficacy of tranexamic acid (TXA), given via intra-articular injection at the time of surgery in patients undergoing the Latarjet procedure for shoulder instability.

NCT ID: NCT02060227 Completed - Clinical trials for Anterior Shoulder Instability

Approach to Shoulder Instability

Start date: March 5, 2014
Phase: N/A
Study type: Interventional

The primary research question is to determine whether patients who undergo a stabilization of the shoulder using a novel decision-making algorithm (ISIS Score) have improved disease-specific quality of life at 1 year post-operatively, as measured by the Western Ontario Instability Index (WOSI) compared with patients who undergo stabilization using a conventional decision-making algorithm. Secondary outcomes include the American Shoulder and Elbow Surgeon's (ASES) score, and difference in recurrence rates of dislocation between the two decision-making algorithms.

NCT ID: NCT01620619 Recruiting - Clinical trials for Anterior Shoulder Instability

The Role of Rotator Interval Closure in Bankart Lesion Repair

Start date: February 2010
Phase: N/A
Study type: Interventional

The null hypothesis is that there is no statistical difference between the two treatment groups for any outcome. The investigators suspect that patients who undergo a Bankart lesion repair with rotator interval closure will have lower quality of life and less external rotation compared to patients who undergo a Bankart lesion repair alone. No difference will be observed for recurrence rate between the two treatment groups