MedTrace Logo

Suture Granuloma in Body Contouring Surgery

NCT00223132 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2012-10-25

No results posted yet for this study

Summary

The purpose of this study is to evaluate the effect of different suture material on the incidence of suture granuloma.

Conditions

  • Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck

Interventions

DEVICE

Absorbable sutures

Sponsors & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Principal Investigators

  • Donna Doran · Medtronic - MITG

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-02-28
Primary Completion
2007-04-30
Completion
2007-04-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT00223132 on ClinicalTrials.gov