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Vicryl Plus and Monocryl Plus in Breast Surgery

NCT00830271 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2020-01-30

No results posted yet for this study

Summary

This is a randomised pilot study comparing conventional sutures (Vicryl and Monocryl) with antiseptic coated equivalents (Vicryl plus andf Monocryl plus) in elective breast surgery.

Conditions

  • Breast Cancer Surgery

Interventions

DEVICE

Vicryl plus and Monocryl plus

closure of skin and subcutaneous tissues

DEVICE

wound closure with Vicryl and Monocryl

wound closure skin and subcutaneous tissues

Sponsors & Collaborators

  • Cardiff and Vale University Health Board

    lead OTHER_GOV

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2011-04-30
Completion
2011-04-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00830271 on ClinicalTrials.gov