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NCT01101789 Clinical Trial

Triclosan Coated Suture Wound Closure for Peripheral Vascular Surgery: a Prospective Multicenter Study

Surgical Wound Infection Clinical Trial

Official title:
Triclosan Coated Suture Wound Closure for Peripheral Vascular Surgery: a Prospective Multicenter Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01101789
Other study ID # NKCH-surg-006
Secondary ID
Status Completed
Phase N/A
First received April 8, 2010
Last updated October 11, 2015
Start date April 2010
Est. completion date January 2011

Study information
Verified date October 2015
Source North Karelia Central Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: North Carelia central hospital, department of vascular surgery
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 276
Est. completion date January 2011
Est. primary completion date January 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- patient undergoing peripheral vascular surgery procedure

Exclusion Criteria:

- patients refusal

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• triclosan coated suture for surgical wound closure
triclosan coated suture for surgical wound closure
• regular sutures for surgical wound closure

Locations
Country Name City State
Finland North Carelia central hospital Joensuu

Sponsors (1)
Lead Sponsor Collaborator
North Karelia Central Hospital

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary surgical wound infection one month after surgical procedure Yes
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