At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Prospective Randomized Controlled Trial Comparing Resident Performance and Clinical Outcomes With Two Different Polypropylene Meshes for Laparoscopic Inguinal Hernias
In Brief
A clinical study evaluating ULTRAPRO Mesh, 3DMAX, and 1 other intervention for Hernia, Inguinal. Completed, enrolled 75 participants across 1 site.
Detailed Summary
The purpose of this research study is to measure the clinical effectiveness of two different polypropylene meshes used for laparoscopic inguinal hernias by evaluating subjects' length of hospital stay, perioperative complications, recurrence rate, pain score, comfort level and postoperative quality of life. A secondary goal of the study is to evaluate the ease of use and time it takes surgical residents to place the mesh and perform the surgery using these two different meshes.
Study Details
Timeline
Interventions
Patients who are randomized to this group will received ULTRAPRO Mesh for their hernia repair
Patients who are randomized to this group will receive 3DMAX mesh for their hernia repair
To evaluate the ease of use and time it takes residents to place and perform the surgery using these two different meshes.