Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2079 participants
OBSERVATIONAL
2012-01-31
2013-12-31
Brief Summary
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Detailed Description
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Design A prospective, multi-center, observational registry. Subject Population Adult, male or female subjects with symptomatic stable angina visiting non-interventional consulting physicians for treatment and who meet the study inclusion/exclusion criteria.
Enrollment:
The study is expected to enroll 1000 to 1500 subjects by 150 - 250 non-interventional consulting physicians. The enrollment period will be around 4 months.
Inclusion criteria
Subject must meet all of the following criteria to be eligible for inclusion in the trial:
1. Subject has been provisionally diagnosed with stable angina by the CP (consulting physician) during the current visit or within 3 months preceding the current visit
2. Subject agrees to sign a data release form
Exclusion criteria
Subjects will be excluded from the trial if any of the following criteria are met:
1. Subject has a history of Acute Coronary Syndrome
2. Subject has a history of prior revascularization
3. Subject has a history of previous MI
4. Subject has new onset angina with symptoms less than one month
Objectives:
1. Describe the demographic and medical profile of subjects diagnosed with stable angina by non-interventional consulting physicians in India
2. Describe the diagnostic pathway prescribed by non-interventional consulting physicians and adopted by stable angina subjects in India
3. Describe the management of stable angina by non-interventional consulting physicians and undertaken by subjects in India
Conditions
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Study Design
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PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
1. Subject has been provisionally diagnosed with stable angina by the CP (consulting physician) during the current visit or within 3 months preceding the current visit
2. Subject agrees to sign a data release form
Exclusion Criteria
1. Subject has a history of Acute Coronary Syndrome
2. Subject has a history of prior revascularization
3. Subject has a history of previous MI
4. Subject has new onset angina with symptoms less than one month
18 Years
ALL
No
Sponsors
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Medtronic Vascular
INDUSTRY
Responsible Party
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Locations
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East Delhi Clinic
New Delhi, New Delhi, India
Countries
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Other Identifiers
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10037399DOC
Identifier Type: -
Identifier Source: org_study_id
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