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

Sponsor
Unity Health Toronto (Other)
Overall Status
Terminated
CT.gov ID
NCT02197819
Collaborator
(none)
3
1
2
60
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Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Sling
  • Device: External Rotation Brace
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
3 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Randomized Evaluation of Emergent Immobilization in External Rotation in the Management of Acute Anterior Dislocations of the Shoulder
Actual Study Start Date :
Feb 1, 2013
Actual Primary Completion Date :
Feb 1, 2018
Actual Study Completion Date :
Feb 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: External Rotation Brace

Shoulder placed in an external rotation brace for 4 weeks

Device: External Rotation Brace

Active Comparator: Traditional Sling

Patient placed in traditional sling

Device: Sling

Outcome Measures

Primary Outcome Measures

  1. Re-dislocation of shoulder [within 12 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Skeletally mature patients between 18 - 35 years of age inclusive

  • Patient is seen within 24 hours from time of injury.

  • Sustained an acute, first-time, traumatic anterior dislocation of the shoulder as defined by;

  • Mechanism of abduction, external rotation

  • Sudden pain in the shoulder

  • Manipulative reduction required or

  • Radiograph documenting a dislocated joint

  • Willing to participate in follow-up for at least 24 months.

Exclusion Criteria:
  • Incompetent or unwilling to consent

  • Inability or unwillingness to comply with rehabilitative protocol or required follow-up assessments.

  • Previous instability of the affected shoulder

  • Significant associated fracture (Exception Hill Sachs or bankart lesions)

  • Concomitant ipsilateral upper extremity injuries which may affect the patient's ability to participate in, or benefit from, a rehabilitative program.

  • Neurovascular compromise of the affected limb

  • A medical condition making the patient unable to wear a brace or sling

  • Patient is seen within 24 hours from time of injury

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Michael's Hospital Toronto Ontario Canada M5C1R6

Sponsors and Collaborators

  • Unity Health Toronto

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Unity Health Toronto
ClinicalTrials.gov Identifier:
NCT02197819
Other Study ID Numbers:
  • EERAADS
First Posted:
Jul 23, 2014
Last Update Posted:
Apr 4, 2019
Last Verified:
Apr 1, 2018
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 4, 2019