Viewing Study NCT01141335


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Study NCT ID: NCT01141335
Status: COMPLETED
Last Update Posted: 2016-11-22
First Post: 2010-06-09
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Polypropylene Mesh Versus Polytetrafluoroethylene (PTFE) Mesh in Inguinal Hernia Repair
Sponsor: University of Roma La Sapienza
Organization:

Study Overview

Official Title: Lichtenstein's Repair of Inguinal Hernia With Polypropylene Mesh Versus InfinitĀ® PTFE Mesh, a Prospective Randomized, Double-blind, Controlled Trial
Status: COMPLETED
Status Verified Date: 2016-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To evaluate the safety and efficacy of the Lichtenstein's hernioplasty using InfinitĀ® PTFE Mesh, and to compare it with the traditional Lichtenstein procedure performed with polypropylene mesh.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: