Triclosan Coated Suture Wound Closure for Peripheral Vascular Surgery: a Prospective Multicenter Study
Overview
This is a prospective randomized multicenter study which purpose is to determine whether triclosan-coated sutures for wound closure after lower limb vascular surgery would reduce the incidence of surgical wound infections.
Study Type
- Study Type: Interventional
- Study Design
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Primary Purpose: Treatment
- Masking: Single (Investigator)
- Study Primary Completion Date: January 2011
Interventions
- Procedure: triclosan coated suture for surgical wound closure
- triclosan coated suture for surgical wound closure
- Procedure: regular sutures for surgical wound closure
Arms, Groups and Cohorts
- Active Comparator: triclosan
- triclosan-coated sutures
- Placebo Comparator: control
- sutures without triclosan-coating
Clinical Trial Outcome Measures
Primary Measures
- surgical wound infection
- Time Frame: one month after surgical procedure
Participating in This Clinical Trial
Inclusion Criteria
- patient undergoing peripheral vascular surgery procedure Exclusion Criteria:
- patients refusal
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: 100 Years
Are Healthy Volunteers Accepted: No
Investigator Details
- Lead Sponsor
- North Karelia Central Hospital
- Provider of Information About this Clinical Study
- Principal Investigator: Sanna Kouhia, MD – North Karelia Central Hospital
- Overall Official(s)
- Johanna Turtiainen, MD, Study Director, North Karelia Central Hospital
- Kimmo Makinen, Principal Investigator, Kuopio University Hospital
- Maarit Venermo, Principal Investigator, Helsinki University Central Hospital
- Eija Saimanen, Principal Investigator, South Carelia Central Hospital
- Ilkka Uurto, Study Director, Tampere University Hospital
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