Prospective Trial Comparing Two Different Polypropylene Meshes for Inguinal Hernias

NACompletedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

June 30, 2014

Primary Completion Date

August 31, 2020

Study Completion Date

August 31, 2020

Conditions
Hernia, Inguinal
Interventions
DEVICE

ULTRAPRO Mesh

Patients who are randomized to this group will received ULTRAPRO Mesh for their hernia repair

DEVICE

3DMAX

Patients who are randomized to this group will receive 3DMAX mesh for their hernia repair

OTHER

Evaluation

To evaluate the ease of use and time it takes residents to place and perform the surgery using these two different meshes.

Trial Locations (1)

28401

New Hanover Regional Medical Center, Wilmington

All Listed Sponsors
collaborator

New Hanover Regional Medical Center

OTHER

lead

South East Area Health Education Center, Wilmington, NC

OTHER

NCT01825187 - Prospective Trial Comparing Two Different Polypropylene Meshes for Inguinal Hernias | Biotech Hunter | Biotech Hunter