BRASD: Biomechanical Reposition techniques in Anterior Shoulder Dislocation. A randomised multicenter clinical trial.

Recruiting

• Conditions: Shoulderdislocation; 10005944

• Registration Number: NL-OMON47421
• Lead Sponsor: Flevoziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 222

Inclusion Criteria

all, legally competent, adult subjects (*18 years) with an isolated anterior shoulder dislocation

Exclusion Criteria

- subcapital humeral fractures
- multi trauma
- subclavicula-, thoracic- , inferior or posterior dislocation
- dislocations presented after 24 hours.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>- length of ED stay in minutes, defined as the moment of arrival at the ED<br /><br>until the patient is discharged<br /><br>- levels of pain experienced by patient before, during and after reduction,<br /><br>measured by NRS (Numeric rating scale (0-10)</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- Time needed for reduction in minutes from start until end of reduction<br /><br>- Numbers of techniques used for reduction<br /><br>- Use of analgesia and/or sedatives (which and dosage), pre-hospital and/or in<br /><br>hospital administered<br /><br>- Pre-reduction status of osseous (x-ray) and neurovascular (physical exam) of<br /><br>the shoulder<br /><br>- Iatrogenic complications (osseous or neurovascular)<br /><br>- Age, gender, ASA classification, last meal (2,4,6 hours, type of meal)<br /><br>- First episode or recurrent dislocation<br /><br>- Trauma mechanism</p><br>