ACTRN12611001286932已完成未知
In patients with idiopathic interstitial pneumonia, nocturnal supplemental oxygen compared with placebo, improves sleep and quality of life
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 30
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
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 80 Years（—）
- 性别
- All
入选标准
- •Patients 18 - 80 yrs.
- •Patients able to perform a polysomnogram (sleep study), as determined following clinical assessment.
- •Patients with nocturnal hypoxaemia, defined as >10% of the night with SpO2 <90% on overnight oximetry or PSG
- •Patients able to give informed consent.
- •Patients with idiopathic interstitial pneumonia (IIP), according to American Thoracic Society /European Respiratory Society criteria.
- •Absence of daytime resting hypoxaemia (ie with PaO2 > 55mmHg).
排除标准
- •Patients <18yrs or >80yrs.
- •Patients not able to give informed consent.
- •Patients considered unable to complete a PSG by their physician.
- •Presence of daytime resting hypoxaemia (PaO2 less than or equal to 55mmHg).
- •Presence of hypercapnia (PaCO2 > 45mmHg) at baseline
- •Patients who do not meet oxygen saturation criteria for nocturnal hypoxaemia
- •Patients with co-existent obstructive sleep apnoea with apnoea hypopnoea index greater than or equal to 15 with clinical symptoms, or apnoea hypopnoea index greater than or equal to 30 (without symptoms)
- •Patients who are current smokers
研究者
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