NCT00572507View on ClinicalTrials.gov

Multi-center Study to Evaluate the Safety and Efficacy of Aesculap MonoMax® for Abdominal Wall Closure

NACompletedINTERVENTIONAL

Enrollment

150

Participants

Timeline

Start Date

December 31, 2007

Primary Completion Date

August 31, 2008

Study Completion Date

July 31, 2009

Conditions

Primary Median Laparotomy

Interventions

DEVICE

MonoMax®

Abdominal wall closure with ultra-longterm absorbable monofilament suture after primary median laparotomy

Trial Locations (4)

35043

Universitaetsklinikum Giessen-Marburg, Klinik fuer Viszeral-, Thorax- und Gefaesschirurgie, Marburg

49808

St. Bonifatius-Hospital; Chirurgische Klinik, Lingen

69120

Universitaetsklinikum Heidelberg, Heidelberg

81377

Universitaetsklinikum Muenchen Grosshadern, München

All Listed Sponsors

lead

Aesculap AG

INDUSTRY

NCT00572507 - Multi-center Study to Evaluate the Safety and Efficacy of Aesculap MonoMax® for Abdominal Wall Closure | Biotech Hunter | Biotech Hunter