Outcomes of Motion-preserving Surgery and Arthrodesis at the Distal Interphalangeal (DIP) Joint
NCT ID: NCT03074916
Last Updated: 2018-04-26
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
52 participants
OBSERVATIONAL
2017-03-08
2018-04-18
Brief Summary
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The primary endpoint is the satisfaction with the treatment result of in the motion-preserving DIP surgery at follow-up.
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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DIP arthroplasty
DIP arthroplasty or arthrodesis
Arthroplasty of the DIP Joint or arthrodesis of the DIP joint
DIP arthrodesis
DIP arthroplasty or arthrodesis
Arthroplasty of the DIP Joint or arthrodesis of the DIP joint
Interventions
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DIP arthroplasty or arthrodesis
Arthroplasty of the DIP Joint or arthrodesis of the DIP joint
Eligibility Criteria
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Inclusion Criteria
* DIP silicone arthroplasty at least one year ago
* Informed consent as documented by signature
Arthrodesis group:
* Matched patients with an DIP arthrodesis
* Informed consent as documented by signature
Exclusion Criteria
* Silicone arthroplasty at the thumb IP joint
* Major surgery at another joint (PIP arthroplasty, thumb trapeziectomy) less than 6 months ago
* Legal incompetence
* German language barrier to complete the questionnaires
Arthrodesis group:
* Arthroplasty at another DIP joint
* Major surgery at another joint (PIP arthroplasty, thumb trapeziectomy) less than 6 months ago
* Legal incompetence
* German language barrier to complete the questionnaires
18 Years
111 Years
ALL
No
Sponsors
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Schulthess Klinik
OTHER
Responsible Party
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Locations
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Schulthess Klinik
Zurich, , Switzerland
Countries
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Other Identifiers
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DIP_Silicone_retro
Identifier Type: -
Identifier Source: org_study_id
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