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Evaluation of Effects of Rosuvastatin 40mg on Myocardial Ischemia in Subjects With Coronary Artery Disease

Primary Purpose

Myocardial Ischaemia, Coronary Artery Disease

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Rosuvastatin
Cholesterol lowering diet
Sponsored by
AstraZeneca
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myocardial Ischaemia focused on measuring Crestor, Rosuvastatin, Cholesterol, Coronary artery disease, Myocardial ischaemia.

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Evidence of Coronary arterial disease
  • Suffering ischaemic episodes/exercise induced ischaemia
  • Not taking any cholesterol lowering medication

Exclusion Criteria:

  • Unstable angina or heart attack less than one month before trial entry
  • Coronary arterial surgery as defined by protocol
  • Uncontrolled hypertension, diabetes, hypothyroidism or laboratory values as defined by the protocol.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    1

    2

    Arm Description

    Rosuvastatin

    Diet

    Outcomes

    Primary Outcome Measures

    Number of episodes of myocardial ischaemia as assessed by ambulatory electrocardiographic monitoring.

    Secondary Outcome Measures

    Change in duration of ischemic episodes
    Safety
    Several laboratory parameters as detailed in the protocol

    Full Information

    First Posted
    April 8, 2008
    Last Updated
    March 13, 2009
    Sponsor
    AstraZeneca
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00657527
    Brief Title
    Evaluation of Effects of Rosuvastatin 40mg on Myocardial Ischemia in Subjects With Coronary Artery Disease
    Official Title
    An 8-Week Randomized Double Blind Placebo Controlled Multicenter Trial to Evaluate the Effects of Rosuvastatin 40mg on Myocardial Ischemia in Subjects With Coronary Artery Disease.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2009
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2001 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    December 2002 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    AstraZeneca

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to determine whether treatment with 40mg of Rosuvastatin for 8 weeks will reduce the number of episodes of myocardial ischaemia suffered in subjects with coronary artery disease.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Myocardial Ischaemia, Coronary Artery Disease
    Keywords
    Crestor, Rosuvastatin, Cholesterol, Coronary artery disease, Myocardial ischaemia.

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    280 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Experimental
    Arm Description
    Rosuvastatin
    Arm Title
    2
    Arm Type
    No Intervention
    Arm Description
    Diet
    Intervention Type
    Drug
    Intervention Name(s)
    Rosuvastatin
    Other Intervention Name(s)
    Crestor
    Intervention Type
    Behavioral
    Intervention Name(s)
    Cholesterol lowering diet
    Primary Outcome Measure Information:
    Title
    Number of episodes of myocardial ischaemia as assessed by ambulatory electrocardiographic monitoring.
    Time Frame
    8 weekly
    Secondary Outcome Measure Information:
    Title
    Change in duration of ischemic episodes
    Time Frame
    8 weekly
    Title
    Safety
    Time Frame
    8 weekly
    Title
    Several laboratory parameters as detailed in the protocol
    Time Frame
    8 weekly

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Evidence of Coronary arterial disease Suffering ischaemic episodes/exercise induced ischaemia Not taking any cholesterol lowering medication Exclusion Criteria: Unstable angina or heart attack less than one month before trial entry Coronary arterial surgery as defined by protocol Uncontrolled hypertension, diabetes, hypothyroidism or laboratory values as defined by the protocol.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michael Cressman, DO
    Organizational Affiliation
    AstraZeneca
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Russell Esterline
    Organizational Affiliation
    AstraZeneca
    Official's Role
    Study Chair

    12. IPD Sharing Statement

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