Skip to content

An observational multicenter study to assess the risk factor profile of early Coronary Artery Disease (CAD) in Indians

A prospective observational study to examine the risk factor profile of premature Coronary Artery Disease (CAD) in Indians

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2012/12/003232
Enrollment
2000
Registered
2012-12-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Risk Factors for CAD

Interventions

None listed

Sponsors

Lotus Clinical Research Academy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients included in the study should satisfy the following criteria. ? Age: Male patients who are less than 55 years and female patients who are less than 65 years of age ? Symptomatic for CAD or established CAD by one or all of the methods described in Section 5.1. ? Willing to sign an informed consent

Exclusion criteria

Exclusion criteria: 1.Age: Male patients who are greater than 55 years and female patients who are greater than 65 years of age 2. There is an absence of CAD or diagnosis of CAD by other methods than those ? by a definite imaging technique ? symptomatic for CAD and stress test positive ? who have had previous Coronary artery bypass surgery (CABG) or Percutaneous Transluminal coronary angioplasty (PTCA). or a doubtful diagnosis of CAD. 3. Unwilling to participate in the study or sign the informed consent

Design outcomes

Primary

MeasureTime frame
risk factor profile of premature CAD in young Indian men (below 55 years) and women (below 65 years).Timepoint: 02 years

Secondary

MeasureTime frame
1.To assess and examine treatment variables and suggested lifestyle changes across regions pre and post-intervention. 2.To compare the prevalence of MI in the study group based on the old and new classification of MI. 3.To assess outcome with reference to practice pattern. 4.To evaluate adherence to guidelines Timepoint: 02 years

Countries

India

Contacts

Public ContactDr S S Iyengar

Scientific Advisor-Lotus Clinical Research Academy Pvt Ltd,

shamiyengar@airtelmail.in09845116933

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026