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LACH-Trial: LAparoscopic Correction of Hernia

NCT00537927 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 215

Last updated 2009-02-18

No results posted yet for this study

Summary

Method of fixation of the mesh in laparoscopic incisional / ventral hernia repair might influence the degree of postoperative pain.

The study hypothesis is that there is no difference in postoperative pain between different methods to fix the mesh in laparoscopic incisional / ventral hernia repair.

Conditions

  • Incisional Hernia
  • Ventral Hernia

Interventions

PROCEDURE

laparoscopic correction of hernia with mesh

Correction of hernia with mesh and fixation of mesh using one of the arms.

Sponsors & Collaborators

  • Ziekenhuisgroep Twente

    lead OTHER

Principal Investigators

  • Eelco B Wassenaar, MD · Ziekenhuisgroep Twente

  • Srjdan Rakic, MD, PhD · Ziekenhuisgroep Twente

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-08-31
Primary Completion
2008-10-31
Completion
2009-01-31

Countries

  • Netherlands

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 NCT00537927 on ClinicalTrials.gov