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临床试验/NCT01753869
NCT01753869终止不适用

Timing of Hypertonic Saline Inhalation Relative to Airways Clearance in Cystic Fibrosis

Belfast Health and Social Care Trust2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2012年12月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
14
试验地点
2
主要终点
Lung Clearance Index

研究概览

简要总结

Lung disease is the predominant cause of morbidity and mortality in Cystic Fibrosis (CF) with 80% of deaths resulting directly or indirectly from pulmonary disease. Abnormal airway clearance causes retention of mucus resulting in frequent chest infections. Physiotherapists use different techniques to help clear mucus from the lungs of patients with CF. Inhaled medications and airways clearance techniques (ACTs) are central to a CF patient's daily treatment and are often coordinated.

Burden of treatment is a common reason for non-adherence in this patient group, and streamlining of treatment timings is sought to optimize adherence whilst ensuring efficacy to an often complex daily regimen of inhaled bronchodilators, nebulizers and ACTs. A gap in the research exists as to the optimal timing of Hypertonic Saline (HTS) and ACT within the daily regimen. A study to show whether the timing of HTS around ACT is significant, can better inform patients and potentially allow more flexibility around their treatment regimen.

Lung Clearance Index (LCI) has shown good sensitivity to abnormalities in lung function compared with spirometry and has demonstrated a treatment effect in other trials. LCI may be a suitable tool therefore, to assess intervention strategies aimed at airways clearance in CF. This study aims to compare the effects ACTs after HTS inhalation versus ACTs during HTS inhalation as measured by LCI.

It is a randomized, crossover trial of ACTs after HTS inhalation compared with ACTs during HTS inhalation in adult CF patients during day 10-14 of a hospital admission for treatment of a pulmonary exacerbation. Patients will be randomized to receive 1 of the treatment session options on the first day and the reverse on the second day.

The primary objective of this study is to compare the change in LCI (a measure of lung function) at 90 minutes post treatment with ACTs after HTS inhalation compared with ACTs during HTS inhalation in adult CF patients.

LCI (lung clearance index) ACT (airway clearance technique) HTS (hypertonic saline)

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (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

  • Male or female patients with a documented diagnosis of CF aged ≥18 years.
  • Written informed consent.
  • At least day 10 - 14 of IV antibiotic therapy during a hospital admission for a pulmonary exacerbation.
  • Patients must be able to perform acceptable spirometric manoeuvres, according to the American Thoracic Society/ERS (ATS/ERS) standards (Miller, Hankinson et. al. 2005).
  • Patient with an FEV1% predicted of ≥ 40%predicted (Stanojevic, Wade et al. 2008).
  • Patients who are productive of sputum from screening visit to study visit 1 (≥10g over 24 hours).
  • Patients who have been prescribed HTS (Nebusal 7%) and have successfully completed a challenge test.
  • Any other chronic medication must have commenced therapy 4 weeks prior to screening and be willing to continue this therapy for the entire duration of the study.

排除标准

  • Day 1-9 of IV antibiotic therapy during a hospital admission.
  • Patients who are colonized with Burkholderia cepacia complex.
  • Patient who are HTS naive.
  • Patients who have an intolerance to HTS.
  • Patients who are currently participating in another study or have participated in another study with an investigational drug within one month of screening.
  • Clinically significant disease or medical condition other than CF or CF-related conditions that, in the opinion of the Investigator, would compromise the safety of the patient or the quality of the data.

结局指标

主要结局

Lung Clearance Index

时间窗: 90 minutes post treatment

次要结局

  • 24 hour sputum volume(24 hours post treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Katherine O'Neill

PhD researcher on behalf of PI: Prof Judy Bradley

Queen's University, Belfast

研究点 (2)

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