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Prevention of Parastomal Hernia With a Mesh

NCT00509054 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2008-04-16

No results posted yet for this study

Summary

Parastomal hernias are randomised to either a conventional stoma formed through the rectus anterior muscle or to the same procedure with the addition of a prophylactic mesh in a sublay position.

Conditions

  • Parastomal Hernia

Interventions

PROCEDURE

Prophylactic mesh

A low weigth partly absorbable mesh in a subaly posistion

Sponsors & Collaborators

  • Sundsvall Hospital

    lead OTHER

Principal Investigators

  • Leif A Israelsson, MD,PhD · Umea University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-01-31
Primary Completion
2007-06-30
Completion
2007-07-31

Countries

  • Sweden

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 NCT00509054 on ClinicalTrials.gov