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
| Type | Name | Description |
|---|---|---|
| DEVICE | Absorbable 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.