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临床试验/ISRCTN76607611
ISRCTN76607611已完成未知

Comprehensive ascertainment of bleeding in patients prescribed different combinations of dual antiplatelet therapy (DAPT) and triple therapy (TT, DAPT plus an anticoagulant) after coronary interventions in the UK: a population based cohort study (the ADAPTT study)

niversity of Bristol (UK)0 个研究点目标入组 21,961 人开始时间: 2016年2月19日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
21,961

研究概览

简要总结

2022 Results article in https://pubmed.ncbi.nlm.nih.gov/35961692/ Patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) (added 15/08/2022) 2023 Results article in https://doi.org/10.3310/mnjy9014 (added 13/07/2023)

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • Patients will be included if they:
  • 1. Are labelled as ‘acceptable’ for use in research by CPRD (a process that identifies and excludes patients with non-continuous follow up or patients with poor data recording that raises suspicion as to the validity of that patient’s record)
  • 2. Are over 18 years of age
  • 3. Have one year of medical history in CPRD before cohort entry (time of index procedure or event)
  • 4. Have a record of aspirin monotherapy (Asp) or dual antiplatelet therapy (DAPT: aspirin and clopidogrel, AC; aspirin and prasugrel, AP; aspirin and ticagrelor, AT) in the year following the index procedure or event
  • 5. No record of DAPT in the 3 month prior to the index procedure or event

排除标准

  • Participants will excluded if they do not meet the above inclusion criteria

研究者

发起方
niversity of Bristol (UK)

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