Randomized Controlled Trial Comparing Different Closure Methods for Laparoscopic Port Sites

N

New York Presbyterian Hospital

Status

Completed

Conditions

Laparoscopic Cosmesis

Treatments

Procedure: Tissue adhesive

Study type

Interventional

Funder types

Other

Identifiers

NCT00466648
HV-2007

Details and patient eligibility

About

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.

Sex

Female

Ages

16 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

gynecologic laparoscopy patients

Exclusion criteria

known sensitivity to tissue adhesive, antibiotic ointment

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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