Effect of HIgh-flow Therapy in Long-term Oxygen Therapy
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Added high-flow oxygen therapy, Standard care.
- Кому может быть актуально
- Состояния в реестре: Chronic Obstructive Pulmonary Disease Severe, Interstitial Lung Disease, Chronic Respiratory Failure With Hypoxia. Базовые параметры: от 18 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Швеция
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Effect of HIgh-flow Therapy in Long-term Oxygen Therapy (HILOT): A Multicenter, Registry-based, Randomized Clinical Trial
Обзор
This is a registry-based, randomized, controlled clinical trial of the effect of added high-flow oxygen therapy (using the device Lumis HFT) during one year in people with long-term oxygen therapy (LTOT) for chronic obstructive pulmonary disease (COPD) or interstitial lung disease (ILD).
Подробное описание
This is a registry-based, randomized, controlled clinical trial of patients with LTOT for COPD or ILD recruited using the Swedish National Registry for Respiratory Failure (Swedevox) in collaboration with a research network within the Swedish Respiratory Society. The trial evaluates the effect of added high-flow oxygen therapy nighttime to the regular low-flow oxygen therapy compared with regular low-flow oxygen therapy alone up to one year.
The purpose of this project is to improve evidence-based treatment of people with chronic respiratory failure, currently about 2000 patients annually in Sweden, who have high risk of adverse events and mortality.
Вмешательства
- Устройство Added high-flow oxygen therapy
Added high-flow oxygen therapy using the device Lumis HFT during nighttime and at the patient's discretion daytime, with the usual care (low-flow oxygen therapy) the rest of the time. - Другое Standard care
Standard care with low-flow oxygen therapy in accordance with clinical routine.
Первичные конечные точки
- Time to first hospitalization or death from all causes [Срок оценки: 1 year]
Вторичные конечные точки (12)
- Time to first all-cause hospitalization or all-cause death [Срок оценки: 1 year]
- Rate of hospitalizations or death from all causes [Срок оценки: 1 year]
- Hospitalization rate from all causes [Срок оценки: 1 year]
- Hospitalization rate from respiratory disease [Срок оценки: 1 year]
- Number of hospitalized days [Срок оценки: 1 year]
- Hospitalization rate from cardiovascular disease [Срок оценки: 1 year]
- Number of admissions to intensive care unit (ICU) [Срок оценки: 1 year]
- Number of days in ICU [Срок оценки: 1 year]
- Mortality rate from all causes [Срок оценки: 1 year]
- Mortality rate from respiratory disease [Срок оценки: 1 year]
- Mortality rate from cardiovascular disease [Срок оценки: 1 year]
- Time to first exacerbation [Срок оценки: 1 year]
Критерии участия
Критерии включения
- Age 40 years or older
- Ongoing LTOT: prescribed for at least 15 hours per day; and since at least 28 days as registered in Swedevox
- COPD or ILD as main underlying reason for LTOT
- Oxygen concentrator as stationary oxygen source in the home including night-time
- Body mass index (BMI) < 35 kg/m2
Критерии исключения
- Current or previous treatment with home HFOT
- Current treatment with home mechanical ventilation
- Current treatment with home CPAP
- Hospitalized during the last 2 weeks
- Current smoking or contact with flames
- Self-reported average use of the LTOT < 15h per day (24 hours)
- PaCO2 (breathing air at rest) > 8 kPa
- Strong clinical suspicion of obstructive sleep apnea (OSA) or obesity-related hypoventilation syndrome (OHS) (as judged by the responsible staff)
- Inability to participate in the study procedures (as judged by the staff)
- Not eligible for continuing LTOT due to other reason (as judged by the staff)
- Expected survival less than 3 months (as judged by the staff)
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
Швеция · 2 центра
- Research Unit, Blekinge University of Technology — Karlskrona
- Department of Heart, Lung and Clinical Physiology, Örebro University Hospital — Örebro
Публикации
- Sundh J, Ljunggren M, Palm A, Lindberg E, Lavergne F, Weinreich UM, Ahmadi Z, Ekstrom M; HILOT Collaboration Group. Effect of HIgh-Flow Therapy in Long-Term Oxygen Therapy (HILOT): study protocol for a multicentre, registry-based, randomised clinical trial. Trials. 2026 Feb 4;27(1):177. doi: 10.1186/s13063-026-09488-8. PMID 41634827
Идентификаторы
NCT: NCT06247397 · HILOT