Health Condition 1: I248- Other forms of acute ischemic heart disease Health Condition 2: I52- Other heart disorders in diseasesclassified elsewhere
Conditions
Interventions
Intervention1: Group 2: Clopidogrel (75 mg) + Ilaprazole (10 mg) in 30 patients for duration of 21 days
Control Intervention1: Group 1: Clopidogrel (75 mg) + Pantoprazole (40 mg) in 30 patients for
Sponsors
SRM College of Pharmacy, SRM Institute of Science and Technology
Eligibility
Inclusion criteria
Inclusion criteria: Patient diagnosed with Acute coronary syndrome and willing to give informed consent form
Exclusion criteria
Exclusion criteria: Concomitant drugs that affects CYP2C19 metabolism Pregnancy/ Lactating women Patient with liver disease Patient with pscyhiatric disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Monitoring of Platelet Reactivity IndexTimepoint: From Baseline,7th,14th and 21st day | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Monitoring complete blood count parameters of the study enrolled participants 2. Monitoring of any adverse events during the studyTimepoint: From Baseline,7th,14th and 21st day | — |
Countries
India
Contacts
Public ContactDr Damodharan N
SRM College of Pharmacy, SRM Institute of Science and Technology
Outcome results
None listed