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Clinical Evaluation of the GLYDe Dressing for Post-surgical Incision Care

NCT00766727 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2020-12-14

Study results available
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Summary

This study will evaluate a new dressing to be used for post-incision care for abdominoplasty patients. The hypothesis is that this dressing will minimize scar formation.

Conditions

  • Post Surgical Incisions From Abdominoplasty Procedures

Interventions

DEVICE

GLYDe Dressing

Wound dressing intended to minimize scar formation

Sponsors & Collaborators

  • Neodyne Biosciences, Inc.

    lead INDUSTRY

Principal Investigators

  • Michael Longaker, MD · Neodyne Biosciences, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2009-11-30
Completion
2010-03-31
FDA Device
Yes

Countries

  • United States

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 NCT00766727 on ClinicalTrials.gov