Stable Angina Observational Registry

STable Angina obseRvational Registry

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01552109

Acronym

STAR

Enrollment

2079

Registered

2012-03-13

Start date

2012-01-31

Completion date

2013-12-31

Last updated

2014-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stable Angina

Keywords

symptomatic stable angina, subjects with symptomatic stable angina visiting non-interventional consulting physicians for treatment and meets the inclusion/exclusion criteria

Brief summary

The purpose of this study is to describe the clinical profile and current status of the diagnosis and management of stable angina in India by non-interventional consulting physicians (CP) through a large multicenter observational registry.

Detailed description

An observational registry on diagnosis and management of stable angina in India Purpose To describe the clinical profile and current status of the diagnosis and management of stable angina in India by non-interventional consulting physicians (CP) through a large multicenter observational registry. 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

Interventions

None listed

Study design

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Countries

India

Outcome results