Health Condition 1: null- study patients are those who underwent coronary angioplasty for coronary artery disease
Conditions
Interventions
Intervention1: clopidogrel: 300mg , two doses 12 hours apart
Control Intervention1: clopidogrel: 600mg single dose
Sponsors
Dr Maddury Jyotsna Additional Professor of Cardiology NIMS Panjagutta Hyderabad A P
Ajantha pharma LtdMumbaiINDIA
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients undergoing elective stenting for obstructive coronary artery disease. 2.Age group of 20-70 years.
Exclusion criteria
Exclusion criteria: 1.Known cases of hypersensitivity to clopidogrel 2.Patients simultaneously receiving GP 2a3b inhibitors. 3. Patients with thrombocytopenia or any other hematological abnormality. 4. Patient in cardiogenic shock. 5.Patients unwillingness after randomization
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| All cause death, allergic reactions, haemorraghic bleeding, gastrointestinal bleedsTimepoint: 6 - 12 hours prior to intervention to day one post intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| side effect like gastrintestinal and/or nervous and/or allegic manifestationsTimepoint: from 0 hours after drug intake to three days | — |
Countries
India
Contacts
Public ContactRNV Narendra Kumar
Additional Prof. Cardiology
Outcome results
None listed