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Clinical Trials/NCT02915588
NCT02915588
Completed
Not Applicable

Early Active Rehabilitation After Arthroscopic Rotator Cuff Repair: A Prospective Randomized Pilot Study

Johannes Kepler University of Linz1 site in 1 country30 target enrollmentJanuary 2012
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ConditionsFull Thickness Rotator Cuff Tear

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Full Thickness Rotator Cuff Tear
Sponsor
Johannes Kepler University of Linz
Enrollment
30
Locations
1
Primary Endpoint
Change of Constant Murley Score
Status
Completed
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of the study is to compare two different rehabilitation protocols after arthroscopic rotator cuff surgery.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
December 2013
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Johannes Kepler University of Linz
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •surgery of the rotator cuff after full thickness tear
  • •informed consent
  • •understanding german language

Exclusion Criteria

  • •previous surgery of the shoulder
  • •neurological or systemic diseases with impairment of shoulder function

Outcomes

Primary Outcomes

Change of Constant Murley Score

Time Frame: up to 24 weeks

Timepoints: Before surgery; 6, 12, 24 weeks after surgery

Secondary Outcomes

  • Change of DASH Score(up to 24 weeks)
  • Change of Active range of Motion (Flexion, Extension, Abduction, Internal Rotation, External Rotation)(up to 24 weeks)
  • Change of Pain (max; average; rest)(up to 24 weeks)
  • Change of Strength (abduction; external Rotation)(up to 24 weeks)

Study Sites (1)

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