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Clinical Trials/NCT02787395
NCT02787395UnknownNot Applicable

Patients Education of a Self-reduction Technique for Anterior Dislocation of Shoulder

Tel-Aviv Sourasky Medical Center0 sites150 target enrollmentStarted: June 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
150
Primary Endpoint
rate of successfull self reduction

Study Overview

Brief Summary

Anterior dislocation of the shoulder (glenohumeral joint) is one of the most prevalent dislocations. Following a first dislocation recurrence rates of up to 80% have been reported. Many patients will seek medical assistance for reduction of the shoulder after each of these recurrent dislocations. The investigators describe the results of reduction of anterior glenohumeral dislocation using a modified self manipulated Milch technique that can be performed by the patients themselves after simple guidance and demonstration. This method is directed to patients who are not willing or cannot have surgical stabilization and may be in a place where medical assistance is not available.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •anterior shoulder dislocation
  • •acute (24 hours) shoulder dislocation

Exclusion Criteria

  • •shoulder fracture
  • •non-cooperative patient

Arms & Interventions

Milch

Experimental

modified Milch technique for self reduction

Intervention: shoulder dislocation self reduction (Procedure)

Boss Holtzach

Experimental

Boss Holtzach technique for self reduction

Intervention: shoulder dislocation self reduction (Procedure)

Stimson

Experimental

Stimson technique for self reduction

Intervention: shoulder dislocation self reduction (Procedure)

Outcomes

Primary Outcomes

rate of successfull self reduction

Time Frame: 10 minutes

the number/rate of successful reductions using each technique will be calculated

Secondary Outcomes

  • pain using VAS during reduction(10 minutes)
  • patient satisfaction from self reduction process using VAS(10 minutes)

Investigators

Sponsor Class
Other Gov
Responsible Party
Sponsor

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