Optima Coronary Artery Disease (CAD) (Optimal Mechanical Evaluation)

Sponsor
University of Pittsburgh (Other)
Overall Status
Completed
CT.gov ID
NCT00896142
Collaborator
(none)
50
1

Study Details

Study Description

Brief Summary

To evaluate the impact of left ventricular (LV) lead location on LV mechanical function.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    50 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Optima CAD (Optimal Mechanical Evaluation)
    Study Start Date :
    Oct 1, 2006

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No

      Inclusion Criteria

      1. Ischemic Cardiomyopathy

      2. Left ventricular ejection fraction less than 40%

      3. Clinical indication for invasive electrophysiology testing

      4. Patient is at least 18 years of age

      Exclusion Criteria

      1. Unstable angina, acute myocardial infarction and/or revascularization procedure within 3 months

      2. CVA or TIA within the past 6 months

      3. Prosthetic heart valve

      4. Patient is status post heart transplant

      5. Women who are pregnant or with child -bearing potential and who are not on a reliable form of birth control. Women of child-bearing potential are routinely tested for pregnancy as part of the standard of care prior to EPS procedures being performed.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 UPMC Presybterian Pittsburgh Pennsylvania United States 15213

      Sponsors and Collaborators

      • University of Pittsburgh

      Investigators

      • Principal Investigator: David S. Schwartzman, MD, University of Pittsburgh

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      University of Pittsburgh
      ClinicalTrials.gov Identifier:
      NCT00896142
      Other Study ID Numbers:
      • 0601112
      First Posted:
      May 11, 2009
      Last Update Posted:
      Nov 22, 2011
      Last Verified:
      Nov 1, 2011
      Keywords provided by University of Pittsburgh
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Nov 22, 2011