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.

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00517452

Acronym

PRP

Enrollment

Registered

2007-08-17

Start date

2007-05-31

Completion date

2007-12-31

Last updated

2011-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atherosclerosis

Brief summary

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

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

35 Years to 90 Years

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Wound healing	4- 6 weeks post op

Outcome results