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Clinical Trial Summary

This study aims to assess the relationship between overall satisfaction with treatment in a group of randomized patients undergoing elective hand surgery using either absorbable (4-0 Chromic) or non-absorbable (5-0 Nylon) sutures. The investigators will also assess factors associated with wound concerns, pain intensity, magnitude of limitations, and physical function within one month of surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03407820
Study type Interventional
Source University of Texas at Austin
Contact
Status Active, not recruiting
Phase N/A
Start date January 31, 2018
Completion date May 30, 2020

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