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A study to understand treatment patterns and health outcomes in patients with chronic stable angina and Type 2 diabetes.

A Prospective, Observational Real World Evidence Study to Assess Medical Management Patterns And Outcomes in Patients With Chronic Stable Angina, Including those with TYPE 2 Diabetes Mellitus - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/07/113725
Enrollment
500
Registered
2026-07-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: I208- Other forms of angina pectoris

Interventions

Intervention1: NIL: NIL

Sponsors

Abbott Healthcare Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosed with Chronic stable angina 2. Patients who are newly initiated on medical management for chronic stable angina. 3. Patients of chronic stable angina with or without Type 2 Diabetes Mellitus as a comorbidity.

Exclusion criteria

Exclusion criteria: 1. Investigators judgement about their disease status of Chronic Coronary Syndrome. 2. Hospitalizations for acute coronary syndrome i.e. myocardial infarction or unstable angina within the past 3 months. 3. Uncontrolled hypertension, defined as systolic blood pressure greater than equal to 180 mmHg or diastolic blood pressure greater than equal to 100 mmHg, despite ongoing antihypertensive therapy 4. New York Heart Association Class III or IV heart failure 5. Current pregnant or breastfeeding 6. Planned coronary artery revascularization surgical or percutaneous within the next 3 months 7. Severe hepatic or renal impairment, or any other significant chronic medical condition requiring continuous treatment. 8. Use of antianginal therapy within the past 3 months for stable angina.

Design outcomes

Primary

MeasureTime frame
1 Duration of chronic stable angina 2 Demographic variables including a. Age, Sex distribution or Socioeconomic status, b. Presence of comorbid conditions such as hypertension, hypercholesterolemia and DM and CV risk factors including alcohol use and tobacco smoking 3 Patients receiving antianginal medications and reporting change in antianginal treatment 4 Proportion of patients requiring addon therapyTimepoint: 1 or 3 months

Secondary

MeasureTime frame
1. Change from baseline in Canadian Cardiovascular Society angina class at 3 months. 2. Change in number of short acting nitrates consumed per week from baseline to 3 months. 3. Change in the mean number of weekly angina attacks 4. Effectiveness of different anti anginal regimens 1 or more molecules based on the secondary endpointsTimepoint: Baseline 1 month or 3 months

Countries

India

Contacts

Public ContactDr Somesh Bolegave

Abbott Healthcare Private Limited

kalpesh.gawand@abbott.com9820928987

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026