MedTrace Logo

Mesh Fixation With Intraperitoneal Tisseel

NCT00842842 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2015-08-19

No results posted yet for this study

Summary

The purpose of this study is to determine whether mesh fixation in laparoscopic umbilical hernia repair with fibrin glue is superior to tacks in terms of postoperative pain and recovery.

Conditions

  • Postoperative Pain
  • Ventral Hernia

Interventions

PROCEDURE

tack fixation of mesh

tack fixation of mesh

PROCEDURE

glue fixation of mesh

glue fixation of mesh

Sponsors & Collaborators

  • Herlev Hospital

    lead OTHER

Principal Investigators

  • Jacob Rosenberg, Professor, D.Sc · Herlev University Hospital, Dept. Surg. Gastroenterology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2010-06-30
Completion
2011-07-31

Countries

  • Denmark

Study Locations

More Related Trials

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 NCT00842842 on ClinicalTrials.gov