PADVa: Peripheral Artery Disease in Vastmanland

Sponsor
Uppsala University (Other)
Overall Status
Completed
CT.gov ID
NCT01452165
Collaborator
Västmanland County Council, Sweden (Other)
457
1
60
7.6

Study Details

Study Description

Brief Summary

The main purposes of this study are:
  • to describe the prevalence and degree of reduced left ventricular function and hypertrophy in patients with peripheral arterial disease in comparison to controls from the general population,

  • to evaluate factors of importance to left ventricular dysfunction and hypertrophy in patients with peripheral arterial disease, and

  • to assess the impact of cardiac function and left ventricular hypertrophy on long-term prognosis in patients with peripheral artery disease.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Left ventricular dysfunction is often a consequence of coronary heart disease (CHD). CHD is prevalent among patients with peripheral artery disease. However, there is limited data regarding left ventricular morphology and function in those patients. In the cross-sectional part of this study we will describe the prevalence of reduced cardiac function and left ventricular hypertrophy in a cohort of patients with peripheral artery disease. The patient outcomes will be compared to control subjects randomly selected from the general population in a case-control design. Further, clinical and genetic determinants of cardiac dysfunction in the patient cohort will be identified. In the longitudinal part of the study, the impact of cardiac function and morphology on cardiovascular mortality and morbidity will be evaluated in the cohort.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    457 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Observational Study on Cardiac Morphology and Function in Patients With Peripheral Artery Disease in Vastmanland County, Sweden(PADVa).
    Study Start Date :
    May 1, 2006
    Actual Primary Completion Date :
    May 1, 2011
    Actual Study Completion Date :
    May 1, 2011

    Outcome Measures

    Primary Outcome Measures

    1. Left ventricular ejection fraction (cross-sectional outcome measure) [baseline]

      LVEF obtained by echocardiographic biplane disk summation method. In the cross-sectional study, the mean value of LVEF and the prevalence of reduced LVEF (LVEF < 50%) in the patient group will be compared to the control group.

    2. Cardiovascular events (longitudinal outcome measure) [5-10 years]

      Cardiovascular events obtained from the Swedish National Causes of Death register and the Swedish National In-patient register. The registers are linked to the patients by the unique personal identification number assigned to each swedish resident.

    3. Left ventricular mass (cross-sectional outcome measure) [baseline]

      Left ventricular mass obtained by 2-dimensional echocardiography according to the American Society of Echocardiography.

    Secondary Outcome Measures

    1. Wall motion score index (WMSI) [baseline]

      Left ventricular wall motion score according to the American Society of Echocardiopgraphy.

    2. Echocardiographic left ventricular filling variables [baseline]

      Echocardiographic variables for evaluation of left ventricular diastolic function (e.g. E/A- and E/e'-ratios).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    Fulfillment of at least one of the following criteria:
    • ankle-brachial-index (ABI) <= 0.9, or

    • stenosis of > 30% of the internal carotid artery, or

    • symptoms typical for claudication and corresponding stenotic findings on the ultrasound examination.

    Exclusion Criteria:
    • age less than 18 years

    • severly impaired communication capabilities

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Center of Clinical Research, Uppsala university, Central Hospital Västerås Sweden SE-72189

    Sponsors and Collaborators

    • Uppsala University
    • Västmanland County Council, Sweden

    Investigators

    • Study Chair: Pär Hedberg, Assoc. Professor, Center of Clinical Research, Uppsala university, Central Hospital, SE-72189 Västerås, Sweden
    • Principal Investigator: Jerzy Leppert, Senior Professor, Center of Clincial Research, Uppsala university, Central Hospital, SE-72189 Västerås, Sweden

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Uppsala University
    ClinicalTrials.gov Identifier:
    NCT01452165
    Other Study ID Numbers:
    • PADVa
    First Posted:
    Oct 14, 2011
    Last Update Posted:
    May 8, 2020
    Last Verified:
    May 1, 2020

    Study Results

    No Results Posted as of May 8, 2020