跳至主要内容
临床试验/ACTRN12621000853842
ACTRN12621000853842已完成未知

Tolerability study of rhinothermy in healthy participants delivered by nasal high flow therapy (rNHF) at 41°Celsius and 45°Celsius

Fisher & Paykel Healthcare Limited0 个研究点目标入组 20 人开始时间: 2021年7月2日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
20

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 75 Years(—)
性别
All

入选标准

  • Twenty healthy participants aged 18 to 75 years who are in the Investigator’s opinion, able and willing to comply with all study requirements.
  • Two weeks post full vaccination against SARS-CoV-2 (COVID-19); may either be New Zealand based COMINARTY (Pfizer BioNTech) or administration of equivalent vaccination

排除标准

  • Upper respiratory tract infection (sore throat, cough, rhinorrhoea and/or fever (subjective of objective) within the last fourteen days
  • Chronic respiratory illness currently being treated e.g. asthma
  • Nasopharyngeal conditions such as a deviated septum and acute/chronic rhinitis, which the investigator considers could impair nasal breathing
  • Use of nasal sprays within the last seven days
  • Current smoker, defined as someone who has smoked or vaped within the last 28 days
  • Current use of or requirement of oral antibiotics for a respiratory tract infection, pneumonia or infective exacerbation of an underlying respiratory condition
  • Current use of or requirement of parenteral antibiotics
  • Have an implantable medical device
  • Have any other condition which, at the investigator’s discretion, is believed may present a safety risk to the participant or others, or impact the study results or the feasibility of the study.
  • Previous enrolment in any trials investigating the use of rhinothermy.

研究者

相似试验