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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms

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

NCT number NCT00223132
Study type Interventional
Source Medtronic - MITG
Contact
Status Completed
Phase Phase 4
Start date February 2005
Completion date April 2007