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临床试验/NCT01586728
NCT01586728终止不适用

Indication and Benefits of Nocturnal Oxygen Therapy in Cystic Fibrosis

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2012年10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
8
试验地点
2
主要终点
the improvement in nocturnal hypoxemia by the measurement of nocturnal pulse oximetry (SpO2) after 6 weeks of nocturnal oxygen therapy in stable patients with CF

研究概览

简要总结

This is an open, multicenter, prospective, randomised and cross over study, comparing in patients with cystic fibrosis aged > 6 years, 2 periods of 6 weeks of oxygen therapy or room air, separated by a wash out period of 2 to 6 weeks.

详细描述

Rationale Oxygen therapy may be proposed to patients with cystic fibrosis (CF) with nocturnal hypoxemia but the indication and benefits of oxygen therapy have not been validated in CF.

Aim of the study and main objective The aim of the study is to evaluate the improvement in nocturnal hypoxemia by the measurement of nocturnal pulse oximetry (SpO2) after 6 weeks of nocturnal oxygen therapy in stable patients with CF.

An improvement is defined by a nocturnal SpO2 > 90% during the whole night.

Objectives and secondary aims

  • Comparison of subjective sleep quality during oxygen therapy and room air after a period of 6 weeks by means of 4 validated sleep questionnaires
  • Comparison of quality of life during oxygen therapy and room air after a period of 6 weeks by means of a validated questionnaire for CF patients (CFQ).
  • Detection of the appearance or increase in nocturnal hypercapnia during oxygen therapy and room air after a period of 6 weeks
  • Comparison of a possible arterial pulmonary hypertension during oxygen therapy and room air after a period of 6 weeks by means of an echocardiography

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
None

入排标准

年龄范围
6 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Children ≥ 6 years and adults ≥ 18 years with CF in a stable state
  • With a forced expiratory volume in one second (FEV1) ≤ 50% of predicted value
  • Having a pulse oximetry (SpO2) in room air ≤ 90% for ≥ 10% of the night and/or a SpO2 ≤ 90% for ≥ 10 minutes during the night
  • Any patient with prior noninvasive positive pressure ventilation (NPPV) but who has stopped NPPV at least 15 days before the start of the study.
  • Written approval by the patient and by the parents in case of a pediatric patient
  • Patient having the French social security coverage

排除标准

  • Patients with a respiratory exacerbation during the last 15 days
  • Patients with NPPV or long term oxygen therapy prior to the start of the study and unable to stop this treatment
  • Impossibility of a medical examination
  • Pregnant patient or breastfeeding patient

结局指标

主要结局

the improvement in nocturnal hypoxemia by the measurement of nocturnal pulse oximetry (SpO2) after 6 weeks of nocturnal oxygen therapy in stable patients with CF

时间窗: after a 6 weeks period

次要结局

  • Comparison of subjective sleep quality during oxygen therapy and room air after a period of 6 weeks by means of 4 validated sleep questionnaires(after a 6 weeks period)
  • Comparison of quality of life during oxygen therapy and room air after a period of 6 weeks by means of a validated questionnaire for CF patients (CFQ).(after a 6 weeks period)
  • Detection of the appearance or increase in nocturnal hypercapnia during oxygen therapy and room air after a period of 6 weeks(after a 6 weeks period)
  • Comparison of a possible arterial pulmonary hypertension during oxygen therapy and room air after a period of 6 weeks by means of an echocardiography(after a 6 weeks period)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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