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临床试验/ACTRN12618000306213
ACTRN12618000306213已完成4 期

Investigating the impact of regular cardio selective beta blockers on recovery with beta agonists following methacholine bronchoconstriction challenge in Asthmatics

Waikato District Health Board, Respiratory Research Fund0 个研究点目标入组 21 人开始时间: 2018年3月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
21

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
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Physician diagnosis of asthma
  • Airway hyper responsiveness. Demonstrated with post mannitol ( a 15 percent decrease in FEV1 at a cumulative mannitol dose PD15 <635mg/ml)
  • Over 18 years of age

排除标准

  • Pre spirometry FEV1 < 60% predicted or < 1.5L
  • Dyspnoea at rest
  • Past history of hypotension (baseline BP <100/60)
  • ECG abnormalities that could interfere with the interpretation of the study:
  • HR<60/min
  • Symptomatic hypotension
  • ECG findings of severe 1st degree, or 2nd & 3rd degree heart block (defined as PR interval > 0.28s)
  • LBBB & RBBB are NOT excluded.
  • Known adverse reaction to beta blockers or mannitol
  • On other drugs that commonly interact with beta blockers (amiodarone, verapramil, cimetidine, digoxin, phenytoin)
  • Already taking beta blockers – including eye-drops.
  • Smoking history of >10 pack years
  • Recent exacerbation as defined by oral corticosteroid use/hospitalisation within 6 weeks of recruitment
  • Pregnant (negative pregnancy test required)
  • Under 18 year of age
  • Unsuitability as defined by the study doctor

研究者

发起方
Waikato District Health Board, Respiratory Research Fund

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