Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Synthetic Mesh for Prevention of HernIa After opEn Abdomen cLosure stuDy

The aim of this clinical trial is to evaluate whether placement of a synthetic prophylactic onlay mesh during definitive fascial closure can reduce the incidence of incisional hernia in adult patients managed with an open abdomen approach following emergency surgery. The main questions it aims to answer are: * Does prophylactic mesh placement reduce the incidence of incisional hernia compared with fascial closure without mesh? * Does prophylactic mesh placement influence the occurrence of postoperative complications such as evisceration or surgical site infection? Researchers will compare patients undergoing definitive fascial closure with prophylactic mesh placement to those undergoing fascial closure without mesh in order to determine whether the mesh decreases the incidence of incisional hernia and associated complications. Participants will: * Undergo standard open abdomen management followed by definitive fascial closure. * Be randomly assigned to one of the two study groups: * Definitive fascial closure without prophylactic mesh. * Definitive fascial closure with placement of a synthetic prophylactic onlay mesh. * Attend clinical follow-up visits in the general surgery outpatient clinic. * Undergo clinical evaluations at 1, 6, and 12 months after surgery, including physical examination and, if necessary, imaging studies to detect incisional hernia or postoperative complications.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital San Juan de Dios TenerifeUpdated: Sep 22, 2026
Eligibility criteria

Patients older than 18 years. [+2]

Patients in whom definitive fascial closure cannot be achieved. [+1]

Status: Recruiting

Influence of Suture Type on Emergency Midline Laparotomy Closure

There is no clear recommendation in international guidelines regarding the type of suture to be used for closing emergency midline laparotomies. It is recommended to follow the same principles as in elective surgery, thus performing the closure with a continuous suture of slowly absorbable monofilament 2-0 with small-bites technique. Currently, there are several slowly absorbable sutures available on the market, and our center uses two: PDS® and Monomax®. These two sutures are currently used interchangeably at our institution based on the preferences of each surgeon. Objective: study whether there are differences between these two sutures in the closure of emergency midline laparotomy.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital San Juan de Dios TenerifeUpdated: Mar 11, 2025Locations: 1
Eligibility criteria

>18 years old, patients undergoing emergency midline laparotomy by the General S...

<18 years old, previous midline laparotomy