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Risk assessment of subcutaneous tendon rupture following plate fixation of distal radius fractures

Not Applicable
Conditions
distal radius fracture
Registration Number
JPRN-UMIN000014123
Lead Sponsor
Aizawa Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

The patients underwent removal of hardware for tenosynovitis, tendon rupture, or hardware malposition.

Study & Design

Study Type
Interventional,observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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