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A study on effects of ticagrelor and prasugrel on inflammatory markers, in diabetic patients undergoing percutaneous coronary intervention

A prospective, observational, comparative study on effects of newer P2Y12 receptor antagonists on inflammatory markers, in diabetic patients undergoing percutaneous coronary intervention - Nil

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/06/054193
Enrollment
54
Registered
2023-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E08-E13- Diabetes mellitus Health Condition 2: I20-I25- Ischemic heart diseases

Interventions

Control Intervention1: NIL: NIL Control Intervention2: T. Prasugrel: 60 mg loading dose (pre PCI) followed by 10 mg once daily maintenance dose Control Intervention3: T. Ticagrelor: 180 mg loading dos

Sponsors

Dr Ankita Panigrahy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients aged between 35 - 70 years of either gender. 2.Diabetic patients , with either stable angina, unstable angina or NSTEMI, with the above mentioned drug therapy and planned for PCI. 3.Patients with Thrombolysis In Myocardial Infarction (TIMI) flow grade 3 after PCI.

Exclusion criteria

Exclusion criteria: 1. Patients posted for Coronary bypass surgery. 2. Patients with uncontrolled diabetes 3. History of stroke or transient ischemic attack or intracranial bleeding at any time 4. Patients who had previous cardiac intervention 5. Patients with cardiogenic shock or hypovolemia 6. Left Ventricular Ejection Fraction (LVEF) 7. Patients with ST segment elevated myocardial infarction 8. Patients with chronic kidney disease stage 3 and beyond 9. Patients requiring reintervention in the study period 10. Need for chronic anti coagulation therapy 11. Patients whose liver function test values are more than 2 times the upper limit of normal 12. History of gastrointestinal bleeding within past 6 months 13. Hypersensitivity to study drugs

Design outcomes

Primary

MeasureTime frame
Changes in levels of hsCRP, IL-6,TNF-alpha after 3 months of treatment compared to baseline Safety of the drugsTimepoint: baseline, 4 weeks, 12 weeks

Secondary

MeasureTime frame
Safety- any incidence of bleeding or stent thrombosisTimepoint: 1 month,4 months

Countries

India

Contacts

Public ContactDr Ankita Panigrahy

Nizams institute of medical sciences, Hyderabad

drarunadonepudi@gmail.com9848923036

Outcome results

None listed

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