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Effectiveness of a Lightweight Mesh in the Laparoscopic Prevention of Parastomal Hernia

NCT00908661 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2017-03-27

No results posted yet for this study

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.

Conditions

  • Parastomal Hernia

Interventions

DEVICE

Lightweight polipropilene and poliglecaprone 25 and oxidized cellulose mesh

Lightweight polipropilene and poliglecaprone 25 and oxidized cellulose mesh

Sponsors & Collaborators

  • Hospital Universitari Vall d'Hebron Research Institute

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2010-11-30
Completion
2010-11-30

Countries

  • Spain

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 NCT00908661 on ClinicalTrials.gov