CEC/EPC and Cardiovascular Risk in Renal Transplant Recipients

Sponsor
University of Florida (Other)
Overall Status
Terminated
CT.gov ID
NCT00365833
Collaborator
(none)
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Study Details

Study Description

Brief Summary

We believe that certain cells in the human body (Circulating Endothelial Cells and Endothelial Progenitor Cells) are related to risk of cardiovascular disease. It may be possible to measure levels of these cells in patients who have had a kidney transplant and predict their risk of developing cardiovascular disease.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Coronary disease is one of the most common causes of morbidity and mortality in patients with known chronic renal insufficiency and those with end stage renal disease. Consequently, early detection with markers such as circulating endothelial cells and endothelial progenitor cells has been studied in order to identify vascular function and assess overall cardiovascular risk. Based on current research, there exists a notable increase in Circulating Endothelial Cells (CEC) and a reduction of Endothelial Progenitor Cells (EPC) with renal dysfunction due to endothelial damage. Therefore circulating endothelial cells are a marker for cardiovascular health.

    Renal transplant patients also possess a higher cardiovascular risk than the general population, but have known improvement in survival as compared to patients with ESRD (End Stage Renal Disease). In addition, because of the excellent outcomes, graft and patient survival and even acute rejection are no longer very useful endpoints for clinical studies. The tolerability of transplant drug regimens and the impact of these regimes on cardiovascular health in kidney transplantation has become, consequently, a new focus of research. Currently, no clear long-term analysis has been fulfilled analyzing CEC or EPC in this group of patients. We hypothesize that CEC can serve as biological markers for cardiovascular risk assessment in cadaveric and living renal transplant patients. We eventually hope measurement of these cells can serve as an endpoint in determining cardiovascular outcome in renal transplant patients. Our present study is aimed to get an initial assessment of the kinetics of CEC and EPC in renal transplant recipients just prior to transplant and for the first two years post transplant.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    8 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Circulating Endothelial Cell and Endothelial Progenitor Cell Evaluation of Kidney Transplant Patients
    Study Start Date :
    Jul 1, 2006
    Actual Primary Completion Date :
    Feb 1, 2007
    Actual Study Completion Date :
    Feb 1, 2007

    Arms and Interventions

    Arm Intervention/Treatment
    Recipients of Kidney Transplant

    Patients Transplanted with Live or Deceased Donor's Kidney. Standard of Care treatment pre- and post-transplant.

    Outcome Measures

    Primary Outcome Measures

    1. Cardiovascular Risk Profile [24 months]

      Cardiovascular Risk Profile is defined by calculated Framingham Model

    Secondary Outcome Measures

    1. Rate of Cardiovascular Events Post-Transplant [24 months]

      Measured by Kaplan-Meier analysis and Cox Proportional Hazard Models to correlate CEC and EPC to this outcome.

    2. Rate of Patient Survival Post-Transplant [24 months]

      Measured by Kaplan-Meier analysis and Cox Proportional Hazard Models to correlate CEC and EPC to this outcome.

    3. Rate of Graft Survival Post-Transplant [24 months]

      Measured by Kaplan-Meier analysis and Cox Proportional Hazard Models to correlate CEC and EPC to this outcome.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • kidney transplant recipients

    • kidney/pancreas transplant recipients

    • age 18-80

    Exclusion Criteria:
    • inability to return for follow-up visits

    • multiple organ transplant other than listed above

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Florida Gainesville Florida United States 32610

    Sponsors and Collaborators

    • University of Florida

    Investigators

    • Principal Investigator: Herwig-Ulf Meier-Kriesche, md, University of Florida
    • Principal Investigator: Giselle Guerra, MD, University of Florida

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Florida
    ClinicalTrials.gov Identifier:
    NCT00365833
    Other Study ID Numbers:
    • 217-2006
    First Posted:
    Aug 18, 2006
    Last Update Posted:
    Sep 30, 2011
    Last Verified:
    Sep 1, 2011
    Keywords provided by University of Florida
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 30, 2011