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A clinical trial to study the "EFFECT OF PROTON PUMP INHIBITORS (Esomeprazole, Pantoprazole and Rabeprazole) ON ANTIPLATELET FUNCTION OF CLOPIDOGREL IN CORONARY ARTERY DISEASE PATIENTS"

"EFFECT OF PROTON PUMP INHIBITORS ON ANTIPLATELET FUNCTION OF CLOPIDOGREL IN CORONARY ARTERY DISEASE PATIENTS"

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/10/004067
Enrollment
90
Registered
2013-10-15
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- coronary angiography proven stable patients of coronary artery disease

Interventions

Intervention1: drug trial Esomeprazole, Pantoprazole, Rabeprazole.: Esomeprazole 20 mg BD per oral for 1 month Pantoprazole 40 mg BD per oral for 1 month Rabeprazole 20 mg BD per oral for 1 month Cont

Sponsors

Postgraduate Institute of Medical Education and Research Chandigarh
Lead Sponsor
PGIMER Chandigarh
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: • Age â?? 25- 70 years ( both male and female) • Angiography proven stable cases of CAD who are on antiplatelet therapy i.e. Aspirin and Clopidogrel but not taking any Proton Pump Inhibitor (PPI).

Exclusion criteria

Exclusion criteria: • Acute Coronary Syndrome (ACS) • Known CAD Patients who are on antiplatelets (Aspirin & Clopidogrel) and already taking any PPI • Patients with thrombocytopenia (platelet count • Active pathological bleeding or a history of hereditary or acquired Bleeding disorder • Peptic ulcer disease • Patient on oral anticoagulants • Liver disease • Anaemia (haemoglobin • Pregnancy • Chronic Kidney Disease (CKD) (Creatinine > 2.5 mg/dl)

Design outcomes

Primary

MeasureTime frame
Difference in platelet aggregation with each Proton Pump Inhibitor before and after their introduction in Coronay Artery Disease patients.Timepoint: 4 WEEKS

Secondary

MeasureTime frame
not applicableTimepoint: 4 weeks

Countries

India

Contacts

Public Contactumesh Kumar

Postgraduate Institute of Medical Education and Research, Chandigarh

dr.umeshchandel@ymail.com918872005444

Outcome results

None listed

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