DIG试验概述

Joseph F Collins Sc.D. , Debra Egan M.Sc., M.P.H. , Salim Yusuf M.B.B.S., F.R.C.P. , Rekha Garg M.D., M.S. , William O Williford Ph.D. , Nancy Geller Ph.D. , on behalf of the DIG Investigators
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引用次数: 6

摘要

充血性心力衰竭在美国、加拿大和其他西方国家是一个主要的公共卫生问题。地黄研究组(DIG)试验是一项随机、双盲、安慰剂对照试验,评估地高辛对心力衰竭、左心室射血分数≤0.45、窦性心律正常的患者全因死亡率和心力衰竭住院的影响。它被设计成一个大型的简单试验。在31.5个月的招募期内,在美国和加拿大的302个参与中心有6800名患者进入了主要研究。所有患者至少随访28个月。为了使这项研究取得成功,许多小组必须成功地合作。在本增刊中,我们介绍了组织和开展像DIG这样的大型简单试验的实际方面。
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Overview of the DIG trial

Congestive heart failure is a major public health problem in the United States, Canada, and other Western countries. The Digitalis Investigation Group (DIG) trial was a randomized, double-blind placebo-controlled trial that evaluated the effects of digoxin on all-cause mortality and on hospitalization for heart failure in patients with heart failure and left ventricular ejection fraction ≤0.45 with normal sinus rhythm. It was designed as a large simple trial. There were 6800 patients entered into the main study over a 31.5-month recruitment period at 302 participating centers in the United States and Canada. All patients were followed for a minimum of 28 months. In order for this study to succeed, many groups had to work together successfully. In this supplement, we present practical aspects of organizing and conducting a large simple trial such as DIG.

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