MedTrace Logo

Prevention of Parastomal Hernia by Mesh Placement

NCT02404545 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2017-09-25

Study results available
· View outcomes & findings →

Summary

Concurrent placement of a mesh during formation of ileal conduit will decrease the incidence of parastomal hernia and associated complications.

Conditions

  • Parastomal Hernia

Interventions

DEVICE

Ethicon Physiomesh

Ethicon Physiomesh will be paced at the time of radical cystectomy and ileal conduit.

Sponsors & Collaborators

  • Ethicon, Inc.

    collaborator INDUSTRY

  • University of Miami

    lead OTHER

Principal Investigators

  • Murugesan Manoharan, MD · University of Miami

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2015-08-14
Primary Completion
2016-08-31
Completion
2017-03-31

Countries

  • United States

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 NCT02404545 on ClinicalTrials.gov