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Clinical trial

A Randomised, Multi-center, Prospective, Observer and Patient Blind Study to Evaluate AESCULAP Optilene® Mesh Elastic Versus Ethicon Ultrapro® Mesh in Incisional Hernia Repair

NCT00646334 is registered in ClinicalTrials.gov with Aesculap AG as lead sponsor.

NCT NCT00646334
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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomised, Multi-center, Prospective, Observer and Patient Blind Study to Evaluate AESCULAP Optilene® Mesh Elastic Versus Ethicon Ultrapro® Mesh in Incisional Hernia Repair
Lead sponsor
Aesculap AG
Phase
Not applicable
Overall status
Completed
Start date
June 30, 2006
Completion date
September 30, 2010
Enrollment
80 (actual)
Sites
6

Conditions

As the registry lists them; a condition with its own page is linked.

incisional hernia repair