跳至主要内容
临床试验/CTRI/2025/08/093318
CTRI/2025/08/093318尚未招募不适用

A retrospective, Cross-sectional study on Ticagrelor usage pattern and tolerability in acute coronary syndrome (CROSS-TIC)

Torrent Pharmaceuticals Ltd.1 个研究点 分布在 1 个国家目标入组 15,000 人开始时间: 2025年9月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
15,000
试验地点
1
主要终点
1. Proportion of patients with ACS on DAPT of ticagrelor and aspirin

研究概览

简要总结

Acute Coronary Syndrome (ACS) is a life-threatening clinical condition resulting from acute myocardial ischemia, encompassing unstable angina (UA), non-ST-segment elevation myocardial infarction (NSTEMI) and ST-segment elevation myocardial infarction (STEMI). It is most commonly caused by atherosclerotic plaque rupture with subsequent thrombosis and platelet aggregation, necessitating prompt antiplatelet therapy. Dual antiplatelet therapy (DAPT), typically involving aspirin and a P2Y12 receptor inhibitor, is the cornerstone of ACS management. While clopidogrel is widely used, its limitations have led to the use of newer agents like prasugrel and ticagrelor.

This retrospective, clinic-based drug utilization study aims to assess the usage pattern and tolerability of ticagrelor in the management of ACS or in patients with a prior history of myocardial infarction. The study will analyze approximately 15,000 cases across India to better understand ticagrelor’s real-world application and impact in secondary cardiovascular event prevention. Data of male or female patients 18 years and above and patients with history of MI or diagnosed with ACS and treated with ticagrelor will be collected for the study.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Male or female patients 18 years and above
  • Patients with history of MI or diagnosed with ACS and treated with ticagrelor.

排除标准

  • 未提供

结局指标

主要结局

1. Proportion of patients with ACS on DAPT of ticagrelor and aspirin

时间窗: Baseline

次要结局

  • 1. Proportion of patients with ACS on DAPT of ticagrelor & aspirin stratified by treatment duration(2. Tolerability)

研究者

发起方
Torrent Pharmaceuticals Ltd.
申办方类型
Pharmaceutical industry-Indian
责任方
Principal Investigator
主要研究者

Dr Mukesh Gabhane

Torrent Pharmaceuticals Ltd.

研究点 (1)

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