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Fascial Closure clinical trials

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NCT ID: NCT04999670 Not yet recruiting - Pregnancy Related Clinical Trials

Fascial Closure and Post-caesarean Pain

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

This study will evaluate post-operative pain in patients undergoing elective caesarean sections based on the method of fascial closure. Patients will be randomised into one of three groups based upon the method of fascial closure and will be followed up over a 10 week period evaluating analgesia use in the acute setting, and also following up with pain scores using a visual analogue score throughout the follow-up period.

NCT ID: NCT03254056 Completed - Post-operative Pain Clinical Trials

Fascial Closure Techniques Post-Operative Pain Laparoscopy

Start date: October 3, 2017
Phase: N/A
Study type: Interventional

This study compares post-operative incisional pain on post-operative days 1 and 7 who will undergo gynecologic laparoscopic operations. Half of participants will undergo conventional fascial closure, while the other will undergo fascial closure by Berci Fascial Closure (Karl Storz, Belgium).

NCT ID: NCT03111134 Not yet recruiting - Fascial Closure Clinical Trials

A New Abdomen Closure Technology Based on Component Separation: a Prospective Randomized Controlled Trial

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

At present, open-type abdominal surgery is routine access into the abdomen. Median incision is the common choice with open-type abdominal surgery. Layered abdomen-closing is often used at the end-time of the surgery. There are some common postoperative complications, such as incision pain, surgical site infection, surgical incision dehiscence and incisional hernia. The key to reduce the incidence of postoperative complications depends on safe and reliable technology of abdomen-closing. It's usually difficult to close the abdomen after the incisional hernia surgery, and the recurrence of incisional hernia is high. But the recurrence fell off observably when component separation technology was applied to abdomen-closing of incisional hernia. Based on this, we hypothesis that modified-CST applied to abdomen-closing in routine abdominal surgery may improve the quality of wound-healing. In this prospective single-blind randomized controlled trial, traditional abdomen-closing technology and modified-CST will be used to gastric cancer surgery, and the quality of wound-healing will be evaluated to confirm which kind of abdomen-closing technology better.

NCT ID: NCT02145052 Active, not recruiting - Fascial Closure Clinical Trials

Optimal Method of Fascial Closure in High Risk Patients Undergoing Laparotomy

Start date: July 2008
Phase: N/A
Study type: Interventional

The primary objective of this study is to identify the optimal method of fascial closure of a laparotomy incision in high risk patients for intra-abdominal complications. The investigators hypothesize that interrupted closure is associated with decreased complication rates when compared with running/continuous closure. Secondary objectives are to determine the rate of dehiscence in continuous and interrupted suture technique, and to determine the rate of wound infection, hernia formation, and mortality associated with suture technique.

NCT ID: NCT00494793 Completed - Open Abdomen Clinical Trials

Vacuum Assisted Wound Closure (VAWC) and Mesh Mediated Fascial Traction

Start date: April 1, 2006
Phase: N/A
Study type: Interventional

The purpose of this multicenter trial is to prospectively evaluate a novel combination of vacuum assisted wound closure (VAWC) and mesh mediated fascial traction for closure of open abdomens.