Skip to main content
Clinical Trials/DRKS00004462
DRKS00004462
Completed
Not Applicable

Predicting the outcome of conservative treatment with physiotherapy for shoulder pain in the presence of atraumatic partial-thickness tears of the rotator cuff

Teesside University, School of Health and Social Care0 sites70 target enrollmentApril 8, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Teesside University, School of Health and Social Care
Enrollment
70
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 8, 2014
End Date
January 16, 2015
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Teesside University, School of Health and Social Care

Eligibility Criteria

Inclusion Criteria

  • Patients with (local) shoulder pain in the presence of an atraumatic (ultrasonographically detected) partial thickness rotator cuff tear (PTT)
  • Clinical signs of shoulder impingement (e.g. painful arc, positive impingement signs (e.g. Hawkins\-Kennedy))
  • Adults ( \= 18 years)
  • No restrictions on gender
  • Agreement on conservative (i.e. non\-surgical) treatment
  • Ability to speak and comprehend the German language
  • Agreement to participate (signed informed consent)
  • Anticipated availability for follow\-up (living in area of Hamburg)
  • Agreement to physiotherapy in one of the collaborating practices.

Exclusion Criteria

  • Presence of a full thickness rotator cuff tear (FTT) at the affected shoulder
  • Previous substantial shoulder trauma (e.g. shoulder dislocation)
  • Previous surgery for the affected shoulder
  • Previous surgery in the shoulder area that may be causal of or contributory to the current problem (e.g. surgery for breast cancer)
  • Clinical or (if available) radiological evidence of structural joint pathology
  • Significantly restricted passive range of movement (ROM) at the affected shoulder (‘capsulitis\-type disorders’); current shoulder infection
  • Clinical signs of symptomatic acromioclavicular arthritis (e.g. local tenderness, positive provocation tests, e.g. ‘Cross\-Body Adduction Stress’ test)
  • Calcific tendinitis
  • Ultrasonographic evidence of Long Head of Biceps (LHB) tendon subluxation/ dislocation
  • Referred pain from the cervical spine region

Outcomes

Primary Outcomes

Not specified

Similar Trials