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临床试验/ACTRN12611001289909
ACTRN12611001289909尚未招募未知

Comparison of blood pressure lowering efficacy between treatment based on a haemodynamic protocol guided by transcutaneous Doppler ultrasound and standard treatment in patients with poorly controlled (Stage 2) hypertension

The Chinese University of Hong Kong0 个研究点目标入组 202 人开始时间: 2011年12月16日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
202

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Patients aged 18 or above who attend the Emegency Department with mean systolic blood pressure > or =160mmHg or diastolic blood pressure >or =100mmHg at two or more blood pressure measurements at least 20 minutes apart, and on two separate occasions (i.e. 2 different calendar days within a 2-week period).

排除标准

  • 1. The patient is pregnant or lactating.
  • 2.The patient is unable to lie supine for USCOM assessment (e.g. due to shortness of breath, severe back pain, oxygen therapy, deformities or pain).
  • 3.The patient is confused, psychiatrically disturbed, or unable to answer questions or communicate.
  • 4.The patient is likely to be admitted to hospital (except admission to the Emergency Medicine Ward).
  • 5. Hypertensive emergencies (e.g. acute stroke, acute coronary syndromes, acute left ventricular failure, acute aortic dissection, hypertensive encephalopathy.)

研究者

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