NCT01877122View on ClinicalTrials.gov

Comparative Study of Safety and Efficacy of Heavyweight and Partially Absorbable Mesh in Inguinal Hernia Repair

PHASE4CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

April 30, 2013

Primary Completion Date

December 31, 2014

Study Completion Date

December 31, 2014

Conditions
Hernia, Inguinal
Interventions
DEVICE

Proflex® Mesh Mesh implantation

Implantation of mesh in the incision of inguinal area

DEVICE

Marlex® Mesh Implant

Trial Locations (1)

Unknown

Samyang Biopharmaceuticals, Seoul

All Listed Sponsors
lead

Samyang Biopharmaceuticals Corporation

INDUSTRY

NCT01877122 - Comparative Study of Safety and Efficacy of Heavyweight and Partially Absorbable Mesh in Inguinal Hernia Repair | Biotech Hunter | Biotech Hunter