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临床试验/NCT02265068
NCT02265068已完成不适用

Real-TICA Real Life Long-term Adherence to Ticagrelor After PCI for Acute Coronary Syndromes. Evaluation of Antiplatelet Therapy After 12 Months in Patients Undergoing PCI and Treated With Ticagrelor During the Acute Phase of an ACS.

IHF GmbH - Institut für Herzinfarktforschung6 个研究点 分布在 1 个国家目标入组 700 人开始时间: 2014年8月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
700
试验地点
6
主要终点
Treatment outcomes of ACS patients receiving Ticagrelor

研究概览

简要总结

Documentation of long-term data regarding ticagrelor use and evaluation of reasons for discontinuation of ticagrelor in patients with ACS

详细描述

REAL-TICA is a retrospective non-interventional study to assess the long-term use of ticagrelor in patients with ACS and to evaluate the reasons for discontinuation of ticagrelor.

For this purpose, selected sites from the ALKK-PCI registry and the respective patients will be identified. The sites' eligibility for this study includes the frequent use of ticagrelor during the acute phase of ACS. Eligible patients are characterised by the diagnosis of ACS and the use of ticagrelor during PCI.

The eligible sites will be contacted by IHF and asked to contact their eligible patients by letter to obtain informed consent of the patients for the planned 12M follow-up by IHF. A detailed questionnaire on events within the last 12 months, current symptoms, current medication and the use of ticagrelor will be added to the patients' letters. Patients then are asked to return their responses on consent to participate in the study as well as the filled in questionnaire to IHF. Alternatively, patients may choose to receive a telephone call by IHF to answer the detailed questionnaire in person. In case of essential information missing, IHF will contact the primary care physician of the patient directly to obtain information about clinical events and medications.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18
  • ACS (STEMI or NSTE-ACS) with PCI
  • Ticagrelor treatment during the acute phase
  • Written informed consent for participation in the study.

排除标准

  • 未提供

结局指标

主要结局

Treatment outcomes of ACS patients receiving Ticagrelor

时间窗: 12 months

Documentation of Events for ACS patients treated with Ticagrelor with follow-up over 12 months

次要结局

  • Long-term use and premature discontinuation of Ticagrelor treatment(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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