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Platelet Rich Plasma Study in Lower Extremity Bypass Surgery (PRP)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00517452
First Posted: August 17, 2007
Last Update Posted: January 5, 2011
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.
Collaborator:
Zimmer Biomet
Information provided by:
Lawson Health Research Institute
  Purpose
The use of platelet rich plasma will decrease wound infection postop.

Condition Phase
Atherosclerosis Phase 2 Phase 3

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: 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.

Resource links provided by NLM:


Further study details as provided by Lawson Health Research Institute:

Primary Outcome Measures:
  • Wound healing [ Time Frame: 4- 6 weeks post op ]

Enrollment: 81
Study Start Date: May 2007
Study Completion Date: December 2007
Groups/Cohorts
Platelet Rich Plasma
Group received platelet rich plasma and observed over a period of 30 days or until wound closure
Standard Wound Care
Group was treated as per standard care

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   35 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Vascular surgical patients scheduled for elective lower extremity bypass surgery,aortoiliac revascularizations and endovascular AAA repair requiring a groin incision
Criteria

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00517452


Sponsors and Collaborators
Lawson Health Research Institute
Zimmer Biomet
Investigators
Principal Investigator: Kirk D Lawlor London Health Sciences Centre, University of Western Ontario
  More Information

Responsible Party: Dr. K. Lawlor, Lawson Health Research Institute
ClinicalTrials.gov Identifier: NCT00517452     History of Changes
Other Study ID Numbers: R-07-098
First Submitted: August 16, 2007
First Posted: August 17, 2007
Last Update Posted: January 5, 2011
Last Verified: January 2011

Additional relevant MeSH terms:
Atherosclerosis
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases