跳至主要内容
临床试验/NCT00115726
NCT00115726已完成4 期

Randomized Controlled Trial Assessing the Effect of Preoperative Furosemide on Intraoperative Blood Pressure

University of Calgary3 个研究点 分布在 2 个国家目标入组 198 人开始时间: 2000年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
198
试验地点
3
主要终点
Proportion of patients developing hypotension during the operative period. Hypotension is defined based on blood pressure criteria (systolic BP <90 mmHg or 35% drop in mean arterial pressure) (or vasopressor treatment during surgery).

研究概览

简要总结

The purpose of this study is to determine whether continuing or discontinuing furosemide (a diuretic) on the day of elective noncardiac surgery for those who take furosemide on a chronic basis, causes more intraoperative hypotension (low blood pressure) during surgery. Our hypothesis is that the usual practice of continuing furosemide on the day of surgery would contribute to more hypotension during surgery than discontinuing furosemide.

详细描述

A significant proportion of patients who undergo surgery take medications on a chronic basis. Little is known about the effects of these medications on the successful conduct of anesthesia and surgery. Diuretics like furosemide may contribute to low blood pressure during surgery, an outcome associated with cardiovascular complications. However, many patients are recommended to take their diuretics on the day of surgery. We wished to determine if preoperative administration of furosemide contributes to intraoperative hypotension compared to placebo.

Comparison: We conducted a randomized, double blind placebo controlled trial to compare the effect of furosemide with that of placebo on intraoperative hypotension using intraoperative blood pressure recordings in patients who take furosemide chronically and were undergoing noncardiac surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • All adults referred to preoperative assessment clinics by surgeons for elective non-cardiac surgery who routinely take furosemide.
  • Participants must also be able to give informed consent

排除标准

  • Less than 18 years of age
  • Have comorbid conditions with which brief periods of hypotension may be particularly harmful such as: 1) pregnancy; 2) baseline hypotension (systolic <100 mmHg at the preoperative assessment clinic); 3) autonomic dysfunction; 4) severe aortic stenosis.
  • Patients who take furosemide only on an 'as needed basis' rather than 'regularly'.
  • Those patients who take less than 10 mg of furosemide daily
  • Those patients who are undergoing local anesthetic only surgical procedures
  • Patients who are unwilling or unable to give informed consent.

研究组 & 干预措施

1

Experimental

furosemide

干预措施: furosemide (Drug)

2

Placebo Comparator

placebo

干预措施: placebo (Drug)

结局指标

主要结局

Proportion of patients developing hypotension during the operative period. Hypotension is defined based on blood pressure criteria (systolic BP <90 mmHg or 35% drop in mean arterial pressure) (or vasopressor treatment during surgery).

时间窗: hospital stay

次要结局

  • Patients will be followed up for the duration of their hospital stay for the following endpoints: (1) Development of congestive heart failure exacerbation(hospital stay)
  • (2) Total cardiovascular complications: composite of acute myocardial infarction, angina, stroke/TIA, arrhythmia, congestive heart failure or cardiac death.(hospital stay)

研究者

申办方类型
Other

研究点 (3)

Loading locations...

相似试验

Trial Assessing the Effect of Preoperative... | 临床试验