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Intraperitoneal Mesh-Implementation After Laparotomy

NCT01003067 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 267

Last updated 2019-08-15

Study results available
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Summary

Aim of the study is to evaluate the risk reduction of intraperitoneal mesh-implementation after laparotomy (Group 1) in a randomized control trial compared with patients with standard abdominal closure (Everett-suture). This is the primary endpoint. Second endpoints are the feasibility of mesh-implementation even after colorectal surgery, find risk factors for wound infection and incisional hernia.

Conditions

  • Incisional Hernia

Interventions

DEVICE

Mesh implementation

Prophylactic intraperitoneal mesh implantation in laparoscopic surgery to prevent incisional hernia.

Sponsors & Collaborators

  • Kantonsspital Liestal

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2013-05-31
Completion
2020-06-30

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01003067 on ClinicalTrials.gov