The Impact of Clavicular Length Restoration in the Treatment of Non-unions of Clavicular Midshaft and Lateral Fractures
NCT ID: NCT03816436
Last Updated: 2019-04-24
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
46 participants
OBSERVATIONAL
2018-08-17
2018-09-25
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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Follow- up (FU) assessment on clavicular non- union
clavicular midshaft and lateral non- union treated by plate and iliac crest bone grafting
Follow- up (FU) assessment
Follow- up (FU) assessment (clinical examination and patient questionnaires) at least 24 months after surgery (clavicular midshaft and lateral non- union treated by plate and iliac crest bone grafting)
Interventions
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Follow- up (FU) assessment
Follow- up (FU) assessment (clinical examination and patient questionnaires) at least 24 months after surgery (clavicular midshaft and lateral non- union treated by plate and iliac crest bone grafting)
Eligibility Criteria
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Inclusion Criteria
* minimal follow- up of two years after surgery
* written informed consent
Exclusion Criteria
* non- union of pathologic fractures
* current pregnancy
* German language barrier to complete questionnaires
18 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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Andreas Mueller, PD Dr. med
Role: PRINCIPAL_INVESTIGATOR
Orthopädische Universitätsklinik Basel
Locations
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Department of Orthopaedics
Basel, , Switzerland
Schulthess Klinik Zürich
Zurich, , Switzerland
Countries
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Other Identifiers
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2018-00120; ch19Mueller
Identifier Type: -
Identifier Source: org_study_id
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