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Platelet Rich Plasma Study in Lower Extremity Bypass Surgery (PRP)
This study is ongoing, but not recruiting participants.
Study NCT00517452   Information provided by Lawson Health Research Institute
First Received: August 16, 2007   No Changes Posted

August 16, 2007
August 16, 2007
May 2007
 
 
 
No Changes Posted
 
 
 
Platelet Rich Plasma Study in Lower Extremity Bypass Surgery
Phase 2-3 Observational Wound Care Study Comparing Application of Platelet Rich Plasma With Standard of Care Wound Closure in Vascular Patients Requiring a Groin Incision.

The use of platelet rich plasma will decrease wound infection postop.

 
Phase II, Phase III
Observational
Natural History, Longitudinal, Defined Population, Prospective Study
Atherosclerosis
 
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
80
August 2007
 

Inclusion Criteria:

  • Vascular surgical patients scheduled for elective lower extremity bypass surgery,aortoiliac revascularizations and endovascular AAA repair requiring a groin incision Exclusion Criteria:Patients requiring emergent procedures, unable to give informed consent
Both
35 Years to 90 Years
No
Contact information is only displayed when the study is recruiting subjects
 
 
NCT00517452
 
R-07-098
Lawson Health Research Institute
Biomet, Inc.
Principal Investigator: Kirk D Lawlor London Health Sciences Centre, University of Western Ontario
Lawson Health Research Institute
August 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP