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Skin Incision Study - Closure of Skin Incisions in Gynecological Cancer Surgery

NCT00107627 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2009-06-25

No results posted yet for this study

Summary

The Skin Incision Study evaluates the efficacy of skin closure methods: skin staples and subcuticular sutures at 6 weeks and at 3 months following the operation by measuring cosmesis and pain.

Conditions

Interventions

OTHER

Caprosyn subcuticular sutures.

Caprosyn subcuticular sutures.

OTHER

Monocryl subcuticular sutures.

Monocryl subcuticular sutures.

OTHER

Skin staples;

Skin staples;

Sponsors & Collaborators

  • Queensland Centre for Gynaecological Cancer

    lead OTHER_GOV

Principal Investigators

  • Andreas Obermair · Queensland Centre for Gynaecological Cancer

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-03-31
Primary Completion
2006-03-31
Completion
2006-03-31

Countries

  • Australia

Study Locations

More Related Trials

Entities

Diseases

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 NCT00107627 on ClinicalTrials.gov