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Randomized Controlled Trial Comparing Different Closure Methods for Laparoscopic Port Sites

NCT00466648 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2007-04-27

No results posted yet for this study

Summary

This study wishes to compare patient satisfaction and cosmesis of two different closure methods of laparoscopic ports. One method uses tissue adhesive (Dermabond) with a deep sub-cutaneous stitch and a Band-Aid dressing. The comparison method uses a 3.o undyed vicryl transcutaneous stitch, with a Bacitracin and Tegaderm dressing.

Conditions

  • Laparoscopic Cosmesis

Interventions

PROCEDURE

Tissue adhesive

Sponsors & Collaborators

  • New York Presbyterian Hospital

    lead OTHER

Principal Investigators

  • Giuseppe Del Priore · New York Presbyterian Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-03-31
Completion
2007-04-30

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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 NCT00466648 on ClinicalTrials.gov