Platelet Rich Plasma Study in Lower Extremity Bypass Surgery
NCT ID: NCT00517452
Last Updated: 2011-01-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
81 participants
OBSERVATIONAL
2007-05-31
2007-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Platelet Rich Plasma
Group received platelet rich plasma and observed over a period of 30 days or until wound closure
No interventions assigned to this group
Standard Wound Care
Group was treated as per standard care
No interventions assigned to this group
Eligibility Criteria
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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
35 Years
90 Years
ALL
No
Sponsors
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Zimmer Biomet
INDUSTRY
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
OTHER
Responsible Party
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Lawson Health Research Institute
Principal Investigators
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Kirk D Lawlor
Role: PRINCIPAL_INVESTIGATOR
London Health Sciences Centre, University of Western Ontario
Other Identifiers
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R-07-098
Identifier Type: -
Identifier Source: org_study_id
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