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Assessment of effect of proton pump inhibitor in management of atheroscleroticcardiovascular disease

Not Applicable
Conditions
Health Condition 1: I700- Atherosclerosis of aorta
Registration Number
CTRI/2023/03/050170
Lead Sponsor
Dr Reddys Laboratories Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other (Terminated)
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Patients with documented history of atherosclerotic cardiovascular disease using dual antiplatelet drugs along with PPIs

Exclusion Criteria

Patients with a history of peptic ulcer or gastric or duodenal surgery

Patients with erosive esophagitis and gastric-outlet obstruction

Patients treated with multiple anti-ulcer medications

Patients with severe pulmonary, hepatic, or renal disease

Patients with incomplete records

Patients on anticoagulants other than aspirin plus clopidogrel and on PPIs other than rabeprazole, pantoprazole and esomeprazole.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The outcome of co administration of various currently used <br/ ><br>PPIs with dual antiplatelet therapy in <br/ ><br>patients of atherosclerotic cardiovascular <br/ ><br>disease will be analyzed in terms of percentage of Myocardial infarction Stroke Unstable angina Heart failure Rehospitalization for <br/ ><br>cardiovascular related illness <br/ ><br>Repeat percutaneous coronary <br/ ><br>intervention or coronary artery bypass grafting <br/ ><br>Death Bleeding events Stent thrombosisTimepoint: Baseline to end of 12 months
Secondary Outcome Measures
NameTimeMethod
The outcome of <br/ ><br>co administration of rabeprazole vs other <br/ ><br>PPIs (pantoprazole, esomeprazole) with <br/ ><br>dual antiplatelet therapy in patients of atherosclerotic cardiovascular <br/ ><br>disease will be analyzed in terms of percentage of Myocardial infarction Stroke Unstable angina Heart failure Rehospitalization for <br/ ><br>cardiovascular related illness <br/ ><br>Repeat percutaneous coronary <br/ ><br>intervention or coronary artery bypass grafting <br/ ><br>Death Bleeding events Stent thrombosisTimepoint: Baseline to end of 12 months
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