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Postoperative Complication clinical trials

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NCT ID: NCT01583751 Recruiting - Recurrence Clinical Trials

Videoendoscopic Pilonidal Sinus Surgery

videosinus
Start date: March 2011
Phase: Phase 1
Study type: Interventional

This study examines performing pilonidal sinus surgery minimal invasively with videoendoscopic approach.

NCT ID: NCT01141335 Completed - Pain Clinical Trials

Polypropylene Mesh Versus Polytetrafluoroethylene (PTFE) Mesh in Inguinal Hernia Repair

Start date: September 2009
Phase: Phase 4
Study type: Interventional

To evaluate the safety and efficacy of the Lichtenstein's hernioplasty using Infinit® PTFE Mesh, and to compare it with the traditional Lichtenstein procedure performed with polypropylene mesh.

NCT ID: NCT00789659 Withdrawn - Wound Infection Clinical Trials

Incisional Wound Vac in Obese Patients

Start date: December 2010
Phase: N/A
Study type: Interventional

It is the belief of the investigators that the current trends in complication rates associated with fixation of pelvic ring injuries and acetabular fractures in the obese are unacceptable. The overwhelming majority of these complications can be attributed to problems with surgical wound healing. The investigators feel that if a cost effective and easily performed intervention can be prospectively utilized in a specific at-risk orthopaedic trauma population in order to control a potentially devastating complication, then efforts in discovering such an intervention may prove valuable. It is our hypothesis that obese patients treated with V.A.C. therapy after standard closure of trauma-related, operative orthopaedic incisions will have fewer postoperative wound complications.