Rapidly Absorbable Versus Non-absorbable Sutures for Mohs Surgery Repair on the Face: a Randomized Controlled Split-scar Study
NCT ID: NCT01932359
Last Updated: 2015-04-13
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
NA
105 participants
INTERVENTIONAL
2013-10-31
2014-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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rapidly absorbable suture (Vicryl Rapide)
rapidly absorbable suture (Vicryl Rapide)
non-absorbable suture (Ethilon)
non-absorbable suture (Ethilon)
Interventions
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rapidly absorbable suture (Vicryl Rapide)
non-absorbable suture (Ethilon)
Eligibility Criteria
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Inclusion Criteria
* Wound greater than or equal to 4 cm in length
* Subject is willing and capable of cooperating to the extent and degree required by the protocol and will be able to come for follow-up assessments
* Subject has read and signed Subject Information and Informed Consent Form
Exclusion Criteria
* Surgical site outside of face
* Subject to be be treated with radiation therapy after surgery
* Subject is not willing or able to attend for follow-up assessments
18 Years
ALL
No
Sponsors
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University of British Columbia
OTHER
Responsible Party
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Principal Investigators
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David Zloty, MD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Locations
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Department of Dermatology and Skin Science, UBC, Vancouver General Hospital
Vancouver, British Columbia, Canada
Countries
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Other Identifiers
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H13-01961
Identifier Type: -
Identifier Source: org_study_id
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