Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to determine if a mesh is effective in the prevention of a parastomal hernia when a permanent ostomy is performed through a laparoscopic approach.


Clinical Trial Description

Parastomal hernia (PH) is a very common complication after abdominal surgery that requires a permanent ostomy. This type of surgery is usually associated with processes that fall within the scope of Coloproctology.PH is difficult to deal with high rates of recurrence after surgical repair.This type of hernia remains a problem of first order, generating a significant consumption of health and economic resources and determining an impaired quality of life of these patients.Laparoscopic surgery is increasingly used in colorectal surgery.

Also with this type of approach is present the problem of prevention of PH. The use of a mesh in the repair of hernias is not discussed since the placement of a prosthesis significantly reduces the recurrence rate. There are now many types of prosthetic meshes available. A low weight mesh composed of large pores (about 5mm) with a high proportion of absorbable material and a layer of oxidized regenerated cellulose which is placed in the vicinity of the bowel is available on the market (PROCEED ®, Ethicon). The introduction of this low-weight mesh provides a good opportunity to prevent the development of an PH when we use a laparoscopic approach. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00908661
Study type Interventional
Source Hospital Universitari Vall d'Hebron Research Institute
Contact
Status Completed
Phase N/A
Start date November 2007
Completion date November 2010

See also
  Status Clinical Trial Phase
Terminated NCT05514600 - Fascial Defect Closure for Minimally Invasive Parastomal Hernia Repair N/A
Recruiting NCT04311333 - Endostomal Three-dimensional Ultrasonography for Parastomal Hernia N/A
Not yet recruiting NCT06077318 - Comparison of the Sugarbaker and Keyhole Repair for Parastomal Hernia
Completed NCT01380860 - Primary Prevention of Peristomial Hernias Via Parietal Prostheses N/A
Recruiting NCT04282473 - Peristomal Hernia Rate 5 Years After a Terminal Colostomy With the Parietex ™ TCM Parietal Prosthesis Versus Without Mesh
Completed NCT03792243 - Outcomes After Parastomal Hernia Repair
Recruiting NCT01955278 - Role of Prosthetic Mesh in Preventing Parastomal Hernias Phase 3
Terminated NCT00641342 - Prevention of Parastomal Hernia by Primary Mesh Insertion Phase 2/Phase 3
Terminated NCT04966065 - Evaluation of the Parietex TM Parastomal No Hole Mesh for Repair of Parastomal Hernias in End-colostomies
Recruiting NCT04440514 - Endoscopic Preperitoneal Parastomal Hernia Repair (ePauli Repair)
Not yet recruiting NCT04950140 - Randomized Clinical Trial Comparing Conventional Laparoscopic Surgery and Robot-Assisted Laparoscopic Surgery for the Treatment of Parastomal Hernia of the Oncology Patient N/A
Terminated NCT02489175 - Stomaplasty Ring (KoringTM) for Prevention of Parastomal Hernia N/A
Recruiting NCT03667287 - Stoma Hernia Intraperitoneal Full-Thickness Skin N/A
Completed NCT01722565 - Prospective Study of the Use of a Mesh to Prevent Parastomal Hernia After Laparoscopic Abdominoperineal Resection Phase 4
Completed NCT02368873 - the Use of a IPOM Mesh for Prevention of Parastomal Hernia N/A
Completed NCT02233465 - Treating Parastomal Hernia With a Mesh Phase 1/Phase 2
Completed NCT00917995 - Trial Concerning the Frequency of Parastomal Hernia With or Without a Mesh Phase 2/Phase 3
Completed NCT01484743 - Risk Factors for Morbidity After Parastomal Hernia Repair
Completed NCT00509054 - Prevention of Parastomal Hernia With a Mesh Phase 4
Completed NCT04187235 - Laparascopic Keyhole vs Sugarbaker Repair in Parastomal Hernia