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临床试验/NCT02234401
NCT02234401Unknown不适用

A Mixed Methods Study Comparing the Clinical Efficacy With the Patient Experience of Non-invasive Ventilation During an Acute Exacerbation Complicated by Respiratory Failure in Adult Cystic Fibrosis

Manchester Metropolitan University2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2014年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
16
试验地点
2
主要终点
Change in day time carbon dioxide (CO2)

研究概览

简要总结

Cystic Fibrosis (CF) is a life limiting illness. Median predicted UK survival is 41.4 years (UK CF Registry 2011). The commonest cause of death is respiratory failure.

Non invasive ventilation (NIV) is a system which delivers a preset pressure to supplement the size and depth of each breath. It is introduced in CF to manage established respiratory failure. A nose or a mask which covers both the nose and mouth allows flexible ventilation, is used just at night, or for part of the day in addition or for 24 hours as clinical status indicates. It is introduced within a normal ward environment and then continued longterm at home.Once respiratory failure is established longterm noninvasive ventilation is introduced throughout 24 hours and multidisciplinary assessment concludes that the timing is appropriate for the individual.

This study aims to evaluate a potential development of current practice: the use of non invasive ventilation during hospital admission only to enhance recovery from an acute exacerbation which has caused respiratory failure in those individuals where long term non invasive ventilation is not yet indicated. A mixed methods design will allow description of the experience of noninvasive ventilation during a semistructured interview to add to understanding of the results from an experiment designed to measure the differences between noninvasive ventilation and standard care.

Aim: To compare the clinical efficacy with the patient experience of NIV on recovery from an acute respiratory exacerbation complicated by respiratory failure in adult Cystic Fibrosis.

详细描述

Design: The study will use a mixed methodology and it will be in 2 phases. Phase I A group randomised controlled trial

The following measurements will be performed on days 1, 3, 7, 10, 14 and twice weekly until discharge:

The exact timing of measurements will be planned by the participant and the researcher.

All of the outcome measures form part of routine clinical practice except the symptom score; the Cystic Fibrosis Respiratory Symptoms Diary (CFRSD V2.0) (Goss et al., 2009)

  1. Early morning and day time carbon dioxide (CO2) level.
  2. Day time oxygen levels
  3. Lung function Forced Expiratory Volume in 1 second (FEV1) and Forced Vital Capacity (FVC)
  4. Day time resting Respiratory Rate (RR), Heart Rate (HR)
  5. Symptom score CFRSD

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

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

  • Adult Cystic Fibrosis
  • Hospital admission to Pearce Ward Manchester Adult Cystic Fibrosis Centre
  • Acute respiratory exacerbation conforming with a standard definition of pulmonary exacerbation (Fuchs et al 1994).
  • An admission day time CO2 > 6 kilopascal (kPa) on standard therapy
  • Freely given informed consent.-
  • 24.3.15 substantial amendment approval for an admission early morning CO2 > 6 kPa

排除标准

  • A day time CO2 >8.0 kPa
  • respiratory acidosis
  • clinical exclusion by CF consultant physician or clinical psychologist

结局指标

主要结局

Change in day time carbon dioxide (CO2)

时间窗: Day 7

次要结局

  • Symptom score (CFRSD)(days 1,3,5,7,10 and 14)
  • Respiratory Rate(days 1,3,5,7,10 and 14)
  • Heart Rate(Days 1,3,5,7,10 and 14)
  • Lung function (FEV1 and FVC)(Day 7, 14)
  • Early morning oxygen (O2) and CO2 levels(days 1,3,5,7,10 and 14)

研究者

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

Susan C Johnson

Consultant Physiotherapist

Manchester Metropolitan University

研究点 (2)

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