Clinical & Radiological Assessment of Rotator Cuff Healing After Single Row Vs. Double Row Rotator Cuff Repair
NCT ID: NCT03885856
Last Updated: 2020-03-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
24 participants
OBSERVATIONAL
2019-04-03
2019-07-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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single row repair technique
patients surgically treated for rotator cuff lesion by single row repair technique
single row repair technique
single row repair technique
double row repair technique
patients surgically treated for rotator cuff lesion by double row repair technique
double row repair technique
double row repair technique
Interventions
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single row repair technique
single row repair technique
double row repair technique
double row repair technique
Eligibility Criteria
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Inclusion Criteria
* Time lapse from injury to surgery ranges from one day to less than 1 year
* Availability of clinical and radiological outcomes from 6 months to 1 year follow up
Exclusion Criteria
* Patient has frozen shoulder
* Chronically retracted tendons and atrophic rotator cuff muscles
70 Years
ALL
No
Sponsors
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University Hospital, Basel, Switzerland
OTHER
Responsible Party
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Principal Investigators
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Mohy Taha, Dr. med
Role: PRINCIPAL_INVESTIGATOR
Department of Orthopaedics and Traumatology, University Hospital Basel
Locations
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Department of Orthopaedics
Basel, , Switzerland
Countries
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Other Identifiers
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2019-00339; ch19Taha
Identifier Type: -
Identifier Source: org_study_id
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