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临床试验/NCT07656714
NCT07656714已完成不适用

Effect of High-frequency Chest Wall Oscillation (HFCWO) Via Chest Vest Combined With Mechanical Cough Assist Versus Mechanical Cough Assist Alone on Respiratory Infections and Hospital Admissions in Patients With Amyotrophic Lateral Sclerosis Receiving Non-invasive Ventilation: a Randomised Single-blind Pilot Trial

Hospital Universitario Virgen Macarena1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2021年4月15日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
14
试验地点
1

研究概览

简要总结

This pilot randomised single-blind trial evaluated whether adding high-frequency chest wall oscillation (HFCWO) via chest vest (ComfortCough II) to mechanical cough assist improves respiratory outcomes and reduces respiratory infections and hospital admissions compared to mechanical cough assist alone in patients with amyotrophic lateral sclerosis (ALS) receiving non-invasive ventilation.

详细描述

Patients with amyotrophic lateral sclerosis (ALS) receiving non-invasive ventilation (NIV) at the Multidisciplinary ALS Unit of Hospital Universitario Virgen Macarena (Seville, Spain) were randomised to two parallel groups. The experimental group received high-frequency chest wall oscillation (HFCWO) via chest vest (ComfortCough II/CC20) combined with mechanical cough assist, while the control group received mechanical cough assist alone. The intervention period lasted 3 months, followed by 3 months of follow-up. Primary outcomes included respiratory infections and hospital admissions. Secondary outcomes included respiratory function, quality of life, sleep quality, and secretion clearance capacity. The study was approved by the Ethics Committee of Hospital Universitario Virgen Macarena - Virgen del Rocío (code 2020-01) and sponsored by FISEVI (Fundación Pública Andaluza para la Investigación Biosanitaria de Andalucía).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Investigator)

盲法说明

Investigators assessing outcomes were blinded to treatment allocation. Blinding of participants and care providers was not feasible due to the nature of the intervention.

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

  • Confirmed diagnosis of ALS according to the Revised El Escorial criteria
  • Under follow-up at the Multidisciplinary ALS Unit of Hospital Universitario Virgen Macarena
  • Age between 18 and 90 years
  • Peak cough flow less than 270 L/min or forced vital capacity (FVC) less than 80% of predicted
  • Ability to travel to the Neurolab centre

排除标准

  • Need for invasive mechanical ventilation
  • Total dependence on non-invasive ventilation (NIV)
  • Severe bulbar involvement
  • Cognitive impairment
  • Comorbidities incompatible with the intervention: pregnancy, rib fractures, known risk of pneumothorax or pneumomediastinum, cerebrospinal fluid fistula, pneumocephalus, or recent barotrauma

研究者

发起方
Hospital Universitario Virgen Macarena
申办方类型
Other
责任方
Sponsor

研究点 (1)

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