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Shoulder Dislocation clinical trials

View clinical trials related to Shoulder Dislocation.

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NCT ID: NCT05010278 Not yet recruiting - Shoulder Luxation Clinical Trials

Evaluation of Factors Associated With Return to Sports Activity Six Months After Anterior Shoulder Stabilisation With Latarjet.

ERASME
Start date: September 2021
Phase:
Study type: Observational

On a population of sports patients who had undergone a Latarjet operation for post-traumatic anterior shoulder instability, reviewed in consultation 6 months after the operation as part of an ordinary follow-up and divided into two groups according to their current sports practice. Group 1: "SUCCESS": return to the same level in the same sport. Group 2: "FAILURE": return to the same sport with a reduced level or change of sport or significant reduction or cessation of sporting activity.

NCT ID: NCT04992598 Withdrawn - Clinical trials for Shoulder Dislocation

Hypnosis to Reduce Pain and Drugs for Shoulder Dislocation Management

HYPSEM
Start date: June 1, 2024
Phase: N/A
Study type: Interventional

The effectiveness of hypnosis for reducing pain was evaluated in various medical specialities. However, only few studies have demonstrated the efficacy of hypnosis for the management of pain in the emergency medicine. Anteromedial dislocation is a very common Reason for admission in emergency department. Many methods for reduction have been described but there is no consensus on the optimum technique or sedation procedures. Some pain medication and tranquilizers used during a shoulder dislocation management include hemodynamic, respiratory and behavioral adverse effects with the requirement of strengthened surveillance. Hypnosis could provide to reduce sedative and analgesic use during the reduction of anteromedial dislocation. The main objective of this study is to evaluate the efficacy of a hypnosis session for reducing the consumption of analgesic in patient throughout a reduction of shoulder dislocation. The investigators also examine the effect of hypnosis on hemodynamic parameters, patient's pain, patient and practitioner satisfaction, sedative consumption, number of attempts for reduction and length of stay in the emergency department.

NCT ID: NCT04977505 Completed - Clinical trials for Shoulder Dislocation

Absorption Rate and Bone Ingrowth of Absorbable Anchors Used in Shoulder Dislocation

Start date: April 21, 2021
Phase:
Study type: Observational

This study aims to analyze the absorption rate of Pushlock anchors and Gryphon anchors and the bone ingrowth of the anchor channel by consulting the postoperative CT images of patients with recurrent shoulder dislocation completed by myself. The investigators will analyze the influence factors of anchor absorption and bone ingrowth, which will provide a reference for improving anchor design and the improvement of surgical techniques.

NCT ID: NCT04960137 Completed - Clinical trials for Shoulder Dislocation

Shoulder Dislocations Treated With Button Plates and Non-absorbable Suture Anchor

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to conduct a comparative study through clinical trials to verify the safety and efficacy of the products in the experimental group for clinical use.

NCT ID: NCT04952636 Recruiting - Clinical trials for Shoulder Dislocation

A Prospective Comparative Study of Arthroscopic and Open Surgery in Cuistow Procedure

Start date: November 6, 2021
Phase: N/A
Study type: Interventional

To evaluate the clinical outcomes of arthroscopic and open Chinese Unique Inlay Bristow procedure in treating recurrent anterior shoulder instability.

NCT ID: NCT04949217 Completed - Clinical trials for Shoulder Dislocation

An Exploratory Randomized Controlled Study of Arthroscopic Inlay Bristow Procedure for Recurrent Anterior Shoulder Dislocation

Start date: January 17, 2017
Phase: N/A
Study type: Interventional

To evaluate the clinical and radiographic outcomes of arthroscopic inlay bristow procedure in treating recurrent anterior shoulder instability.

NCT ID: NCT04901780 Completed - Shoulder Pain Clinical Trials

Pragmatic Posterior Capsular Stretch

PPCS
Start date: May 5, 2020
Phase: N/A
Study type: Interventional

Various stretches are used to lengthen the posterior shoulder capsule. No study has reported the comparison of the pragmatic posterior capsular stretch and cross body stertch

NCT ID: NCT04887337 Recruiting - Clinical trials for Shoulder Dislocation

Early arthroscoPic Stabilization veRsus rehabilitatiOn of the Shoulder in Adolescents With a trauMatic First-time Anterior Shoulder Dislocation ePisode

PROMPT
Start date: September 19, 2022
Phase: N/A
Study type: Interventional

Each year within Canada and the US, more than 30,000 children and adolescents will have an injury to their shoulder resulting in a shoulder dislocation. Although the current practice is to manage this initial dislocation without surgery, the vast majority of these children and adolescents will, unfortunately continue to have instability episodes of their shoulder. Recurrent instability can cause damage to the bones and cartilage that form the shoulder resulting in potentially more difficult surgical stabilization, and possibly long-term sequela. To that effect, there is increasing interest to consider early surgical stabilization in this population. This pilot randomized controlled trial (RCT) will evaluate the feasibility of conducting a larger RCT assessing the effect of early arthroscopic stabilization compared to rehabilitation on the rate of repeat shoulder dislocations (recurrent instability), pain, and shoulder function among adolescents (aged 12-18 years) with first-time shoulder dislocations. These patients will be followed for one year.

NCT ID: NCT04823689 Recruiting - Emergencies Clinical Trials

Reduction of Anterior Glenohumeral Dislocation in Ventral Decubitus Versus Dorsal Decubitus Under Procedural Sedation

EPOLUX
Start date: July 21, 2021
Phase: N/A
Study type: Interventional

The anterior glenohumeral dislocation is frequently encountered in emergency medicine. It represents about 50% of the total dislocation and affects 1 resident for 10 000 in France. In Nord Franche-Comte Hospital, 1 to 2 patients per day present this diagnosis in the emergency department, which requires reduction by external manoeuvres. A retrospective study shows the interest of the ventral decubitus compared to dorsal decubitus reduction in the care of patients with anterior glenohumeral dislocation. None prospective study has already demonstrate the interest of the ventral decubitus compared to the dorsal decubitus in the reduction of anterior glenohumeral dislocation. The main objective is to evaluate the speed of the reduction of the anterior dislocation of the shoulder by the ventral decubitus technique compared to the conventional technique in dorsal decubitus.

NCT ID: NCT04823455 Active, not recruiting - Clinical trials for Shoulder Dislocation Closed Traumatic

Results Following Fresh-frozen Humeral Head Osteochondral Allograft Reconstruction for Reverse Hill-Sachs Lesion

ALLO-OMERO2020
Start date: June 5, 2020
Phase: N/A
Study type: Interventional

Locked posterior glenohumeral dislocations with a reverse Hill-Sachs impaction fracture involving less than 30% of the humeral head are most frequently treated with lesser tuberosity transfer into the defect, whereas those involving more than 50% undergo humeral head arthroplasty. Reconstruction of the defect with segmental femoral osteochondral allografts has been proposed to treat patients between these two ranges, but the medium-/long-term outcomes of this joint-preserving procedure are controversial.