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Clinical Trials/NL-OMON41074
NL-OMON41074
Withdrawn
Not Applicable

ong term results of arthroscopic debridement of partial rotator cuff ruptures. - LADPARC

Onze Lieve Vrouwe Gasthuis0 sites30 target enrollmentTBD
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Conditionspartial rotator cuff rupture10005944

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
partial rotator cuff rupture
Sponsor
Onze Lieve Vrouwe Gasthuis
Enrollment
30
Status
Withdrawn
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Onze Lieve Vrouwe Gasthuis

Eligibility Criteria

Inclusion Criteria

  • •All patients diagnosed with a partial rotator cuff rupture, confirmed by MRI or ultrasound
  • •All patients who received arthroscopic debridement at the department of orthopaedic surgery of the OLVG between January 2001 and December 2004;
  • •Patients older than 18 years at the moment of diagnosis partial rotator cuff rupture;
  • •Surgical intervention: debridement with or without acromioplasty

Exclusion Criteria

  • •Inadequate knowledge of Dutch language;
  • •Post\-operative incident of ipsilateral shoulder injury such as fractures or AC separation or shoulder dislocation;
  • •Neurological conditions influencing upper limb;
  • •Unable to visit the outpatient clinic to undergo CMS testing;

Outcomes

Primary Outcomes

Not specified

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