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Assessment of antiplatelet resistance in post-angioplasty patients (THE ANTI-PLATELET RESISTANCE STUDY)

ASSESSMENT OF ANTIPLATELET DRUG RESISTANCE IN PATIENTS WITH CORONARY ARTERY DISEASE UNDERGOING PERCUTANEOUS CORONARY INTERVENTION AT A TERTIARY CARE HOSPITAL - APRS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/01/011578
Enrollment
192
Registered
2018-01-29
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- The study will include adult patients (age 18 years) with newly diagnosed CAD for which angioplasty is done with stents

Interventions

None listed

Sponsors

Manipal Academy of Higher Education
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. >=18 years of age, male, or female 2. Patients with newly diagnosed CAD for which coronary angioplasty is done with stent (s) 3. Patients on dual antiplatelet therapy including aspirin and one of the P2Y12 inhibitors i.e. clopidogrel, ticagrelor or prasugrel.

Exclusion criteria

Exclusion criteria: 1. Patients with the history of CAD, CABG and/or angioplasty 2. Hb 3. Patient with decompensated heart failure 4. Patients with metabolic syndrome 5. History of chronic kidney disease 6. History of malignancy 7. History of psychiatric illness 8. History of chronic hepatic disease 9. History of bleeding diathesis 10. Pregnancy and lactation 11. Any other medication that might effects of study drugs eg: rifampicin, phenytoin, carbamazepine 12. Any other medical condition that, in the opinion of the investigator, may be an unacceptable additional risk to the patient 13. Patients on antithrombotic agents including antiplatelet drugs, anticoagulants and thrombolytic drugs for any other reason 14. Patients with history of CVA, TIA, acute or chronic pulmonary embolism or any valvular heart disease for which he/she was on antithrombotic, anticoagulants and antiplatelet drugs 15. Patientâ??s participation in any other clinical trial with an investigational treatment

Design outcomes

Primary

MeasureTime frame
Incidence of antiplatelet drugs resistance in the recruited populationTimepoint: 2 Year (After angioplasty procedure)

Secondary

MeasureTime frame
Assessment of adverse cardiac outcomes (MACE) in post angioplasty patients in view of dual antiplatelet drug resistanceTimepoint: 2 Year (After angioplasty procedure);Assessment of P2Y12 platelet inhibitors associated mortality and comparative mortality analysis between three agents (Clopidogrel, ticagrelor and Prasugrel)Timepoint: 2 Year (After angioplasty procedure)

Countries

India

Contacts

Public ContactDr Tom Devasia

Melaka Manipal Medical College

yashwanthrao2000@gmail.com9880703774

Outcome results

None listed

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