Clinical Trials Directory

Trials / Completed

CompletedNCT00223132

Suture Granuloma in Body Contouring Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
Sponsor
Medtronic - MITG · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

Bariatric surgery has evolved as an effective treatment for morbid obesity, inducing rapid and predictable weight loss within a period of 12 to 18 months following surgery. Consequently, body contouring after weight loss is emerging as the fastest growing field of plastic surgery. Patients seek consultation with a plastic surgeon to correct skin laxity of the abdomen, thighs, chest, back, and neck. A major problem in body contourinig is the extrusion of absorbable suture material used for dermal closure. Long incisions and high tension inherent to body contouring surgery mandate a secure dermal closure. While absorbable sutures are preferred, they can result in suture granuloma and extrusion.

Conditions

Interventions

TypeNameDescription
DEVICEAbsorbable sutures

Timeline

Start date
2005-02-01
Primary completion
2007-04-01
Completion
2007-04-01
First posted
2005-09-22
Last updated
2012-10-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00223132. Inclusion in this directory is not an endorsement.