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NCT00672672 Clinical Trial

Autologous Platelet Gel in Wound Healing of Coronary Artery Bypass Grafting (CABG) Patients

Infection Clinical Trial

Official title:
Autologous Platelet Gel in Wound Healing of Coronary Artery Bypass Grafting (CABG) Patients

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00672672
Other study ID # 0065-08-FB
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 13, 2009
Est. completion date January 6, 2010

Study information
Verified date August 2023
Source University of Nebraska
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will determine if autologous platelet gel (APG) on sternal incision and conduit sites will improve wound healing and decrease infection in coronary artery bypass grafting surgery patients.

Description:

The purpose of this study is to determine if the use of autologous platelet gel (APG) on sternal incision and conduit sites will improve wound healing and decrease the incidence of infection in patients undergoing coronary artery bypass grafting surgery

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 6, 2010
Est. primary completion date January 6, 2010
Accepts healthy volunteers No
Gender All
Age group 19 Years to 90 Years
Eligibility Inclusion Criteria: - Any patient who meets criteria and consents to undergo a CABG procedure involving conduit sites and consents to this study. Exclusion Criteria: - Any patient, after inclusion, whom is later determined to have had on-going therapy that could influence wound healing such as radiation or chemotherapy, extensive steroid use, or accidental trauma such as burns, etc.

Study Design

Related Conditions & MeSH terms

Intervention

Biological:
• autologous platelet gel
Patients will receive APG to the surgical site in the operating room. The control site will receive no treatment.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Nebraska

Outcome
Type Measure Description Time frame Safety issue
Primary Healing and infection of surgical sites The surgical sites will be assessed for degree of healing and signs and symptoms of infection on post-op days one and three and during the patients' follow up visits in the clinic. 30 days
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