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ProLOVE - Prospective Randomized Study of Midline Incisional Hernia Treatment (ProLOVE)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00472537
First Posted: May 11, 2007
Last Update Posted: April 24, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
Region Skåne FoUU
Lund University
Ethicon, Inc.
The Einar & Inga Nilsson Foundation
The Anna-Lisa & Sven-Eric Lundgren Foundation, Malmö Sweden
Crafoord Foundation
Information provided by (Responsible Party):
Peder Rogmark, Skane University Hospital
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: November 2010
  Primary Completion Date: November 2010 (Final data collection date for primary outcome measure)
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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