跳至主要内容
临床试验/NCT04593030
NCT04593030已完成不适用

Replication of the ARISTOTLE Anticoagulant Trial in Healthcare Claims Data

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 220,518 人开始时间: 2020年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
220,518
试验地点
1
主要终点
Relative hazard of composite outcome of Stroke and Systemic Embolism

研究概览

简要总结

Investigators are building an empirical evidence base for real world data through large-scale replication of randomized controlled trials. The investigators' goal is to understand for what types of clinical questions real world data analyses can be conducted with confidence and how to implement such studies.

详细描述

This is a non-randomized, non-interventional study that is part of the RCT DUPLICATE initiative (www.rctduplicate.org) of the Brigham and Women's Hospital, Harvard Medical School. It is intended to replicate, as closely as is possible in healthcare insurance claims data, the trial listed below/above. Although many features of the trial cannot be directly replicated in healthcare claims, key design features, including outcomes, exposures, and inclusion/exclusion criteria, were selected to proxy those features from the trial. Randomization is also not replicable in healthcare claims data but was proxied through a statistical balancing of measured covariates according to standard practice. Investigators assume that the RCT provides the reference standard treatment effect estimate and that failure to replicate RCT findings is indicative of the inadequacy of the healthcare claims data for replication for a range of possible reasons and does not provide information on the validity of the original RCT finding.

研究设计

研究类型
Observational
观察模型
Cohort
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 years
  • Atrial fibrillation - either of the following:
  • 2a. In atrial fibrillation or atrial flutter not due to a reversible cause and documented by ECG at the time of enrollment
  • 2b. If not in atrial fibrillation/flutter at the time of enrollment, must have atrial fibrillation/flutter documented on two separate occasions, not due to a reversible cause at least 2 weeks apart in the 12 months prior to enrollment. Atrial fibrillation/flutter may be documented by ECG, or as an episode lasting at least one minute on a rhythm strip, Holter recording, or intracardiac electrogram (from an implanted pacemaker or defibrillator)
  • One or more of the following risk factor(s) for stroke:
  • 3a. Age 75 years or older
  • 3b. Prior stroke, TIA, or systemic embolus
  • 3c. Either symptomatic congestive heart failure within 3 months or left ventricular dysfunction with an LV ejection fraction (LVEF) ≤ 40% by echocardiography, radionuclide study or contrast angiography
  • 3d. Diabetes mellitus
  • 3e. Hypertension requiring pharmacological treatment

排除标准

  • Clinically significant (moderate or severe) mitral stenosis
  • Increased bleeding risk that is believed to be a contraindication to oral anticoagulation (e.g. previous intracranial hemorrhage)
  • Conditions other than atrial fibrillation that require chronic anticoagulation (e.g. prosthetic mechanical heart valve)
  • Persistent, uncontrolled hypertension (systolic BP > 180 mm Hg, or diastolic BP > 100 mm Hg)
  • Active infective endocarditis
  • Simultaneous treatment with both aspirin and a thienopyridine (e.g., clopidogrel, ticlopidine)
  • Severe comorbid condition with life expectancy of ≤ 1 year
  • Active alcohol or drug abuse, or psychosocial reasons that make study participation impractical
  • Recent ischemic stroke (within 7 days)
  • Severe renal insufficiency (serum creatinine > 2.5 mg/dL or a calculated creatinine clearance < 25 mL/min, See Section 6.3.2.2)
  • Platelet count ≤ 100,000/ mm3
  • Hemoglobin < 9 g/dL
  • Women of child bearing potential (WOCBP) unwilling or unable to use an acceptable method to avoid pregnancy

研究组 & 干预措施

Warfarin

Reference group

干预措施: Warfarin (Drug)

Apixaban

Exposure group

干预措施: Apixaban (Drug)

结局指标

主要结局

Relative hazard of composite outcome of Stroke and Systemic Embolism

时间窗: [Time Frame: Through study completion (a median of 98 days)]

Relative hazard of composite outcome of Stroke and Systemic Embolism - Please refer to uploaded protocol for full definition due to size limitations.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Shirley Vichy Wang

Associate Professor of Medicine

Brigham and Women's Hospital

研究点 (1)

Loading locations...

相似试验