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Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Mesh Fixation

NCT02467140 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2015-06-09

No results posted yet for this study

Summary

A clinical study evaluating acute and chronic pain following laparoscopic inguinal hernia repair comparing the ProGripTM self- fixating mesh with tack fixation.

Conditions

  • Inguinal Hernia
  • Pain

Interventions

DEVICE

Parietex ProGrib self-fixating mesh

Laparoscopic transabdominal preperitoneal inguinal hernioplasty using the Parietex ProGrib self-fixating mesh.

DEVICE

Tack fixation

Laparoscopic transabdominal preperitoneal inguinal hernioplasty using the Parietex ProGrib self-fixating mesh using tack fixation.

Sponsors & Collaborators

  • Medtronic - MITG

    collaborator INDUSTRY

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Michael F Nielsen, MD PhD

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-05-31
Completion
2017-05-31

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Diseases

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 NCT02467140 on ClinicalTrials.gov