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Shoulder Dislocation clinical trials

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NCT ID: NCT04820491 Terminated - Clinical trials for Shoulder Dislocation

Efficient Anterior Shoulder Ultrasound Reduction Multicenter Prospective Randomized Trial

EASiUR
Start date: March 26, 2021
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if using ultrasound to diagnosis and confirm reductions of shoulder dislocations impacts the length of an emergency department visit for this condition.

NCT ID: NCT03245320 Terminated - Clinical trials for Rheumatoid Arthritis

Clinical Evaluation of the TITAN™ Total Shoulder System

Start date: March 20, 2017
Phase:
Study type: Observational

A post market, non-randomized, multi-center, open-label,clinical study using survivorship to study the safety and efficacy of the Integra® TITAN™ Total Shoulder System 1.0 (TAS) when used for total shoulder arthroplasty.

NCT ID: NCT02426996 Terminated - Clinical trials for Shoulder Dislocation

The Latarjet-type Procedure Using the SEM Positioner: Using a Scan to Assess Consolidation

IACE Scan
Start date: May 2016
Phase: N/A
Study type: Interventional

The main objective of this study is to evaluate, after surgery for chronic anterior shoulder instability using a Latarjet technique with positioning of the bone block via an SEM positioning tool, the value of the contribution of a shoulder scan at 3 months post surgery in the decision to return to activity early as conditioned by the quality of the bone block consolidation.

NCT ID: NCT02197819 Terminated - Clinical trials for Primary Anterior Shoulder Dislocation

A Randomized Evaluation of Emergent Immobilization in External Rotation in the Management of Acute Anterior Dislocations of the Shoulder

EERAADS
Start date: February 1, 2013
Phase: N/A
Study type: Interventional

Shoulder dislocations are quite common, the prevalence over a lifetime being estimated at 2% in the general population. In young patients, recurrence after a primary dislocation is also common (~60%) and multiple recurrent episodes can cause significant disability over time. Following initial reduction of the joint, the traditional treatment for primary shoulder dislocations has been immobilization in a sling, with the arm in a position of adduction and internal rotation. The length of the immobilization period is controversial, however most authors would recommend between three to six weeks in a sling followed by several months of rehabilitation to include range of motion and strengthening exercises. The clinical course of patients after this approach has been extensively investigated. Of particular interest is the relatively high rate of recurrent instability in young patients, reported to be between 17 and 96%. A prospective randomized trial is needed to determine whether in young patients (16-30 yrs of age) following reduction of a first-time traumatic anterior shoulder dislocation, does EMERGENT (<4 hours post reduction) immobilization of the affected shoulder in external rotation reduce the rate of recurrent instability experienced within 12 months versus emergent immobilization in a traditional internal rotation sling? Eligible patients will be randomly allocated to the sling or ER brace. The results of this study will provide the best evidence for choosing emergent immobilization for shoulder dislocations.

NCT ID: NCT00326352 Terminated - Clinical trials for Shoulder Dislocation

Comparison of Sedation/Analgesia: Midazolam/Morphine Vs Propofol/Remifentanil

Start date: July 2003
Phase: N/A
Study type: Interventional

For reduction of dislocated shoulder, sedation with propofol and remifentanil should give satisfactory operating conditions and pain relief, and significantly reduce the time to full recovery, compared with morphine and midazolam