REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocol

Abstract Objective Long-term oxygen therapy (LTOT) during 15 h/day or more prolongs survival in patients with chronic obstructive pulmonary disease (COPD) and severe hypoxemia. No randomized controlled trial has evaluated the net effects (benefits or harms) from LTOT 24 h/day compared with 15 h/day...

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Main Authors: Josefin Sundh, Anna Bornefalk-Hermansson, Zainab Ahmadi, Anders Blomberg, Christer Janson, David C. Currow, Christine F. McDonald, Nikki McCaffrey, Magnus Ekström
Format: Article
Language:English
Published: BMC 2019-02-01
Series:BMC Pulmonary Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12890-019-0809-7
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spelling doaj-85a73245cafc4d27a884c0b32ba0675e2020-11-25T02:38:54ZengBMCBMC Pulmonary Medicine1471-24662019-02-011911810.1186/s12890-019-0809-7REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocolJosefin Sundh0Anna Bornefalk-Hermansson1Zainab Ahmadi2Anders Blomberg3Christer Janson4David C. Currow5Christine F. McDonald6Nikki McCaffrey7Magnus Ekström8Department of Respiratory Medicine, School of Medical Sciences, Örebro UniversityUCR Uppsala Clinical Research Center, Uppsala UniversityDepartment of Clinical Sciences, Division of Respiratory Medicine & Allergology, Lund UniversityDepartment of Public Health and Clinical Medicine, Division of Medicine/Respiratory Medicine, Umeå UniversityDepartment of Medical Sciences, Respiratory, Allergy & Sleep Research, Uppsala UniversityFaculty of Health, University of TechnologyInstitute for Breathing and SleepDeakin Health Economics, Deakin UniversityDepartment of Clinical Sciences, Division of Respiratory Medicine & Allergology, Lund UniversityAbstract Objective Long-term oxygen therapy (LTOT) during 15 h/day or more prolongs survival in patients with chronic obstructive pulmonary disease (COPD) and severe hypoxemia. No randomized controlled trial has evaluated the net effects (benefits or harms) from LTOT 24 h/day compared with 15 h/day or the effect in conditions other than COPD. We describe a multicenter, national, phase IV, non-superiority, registry-based, randomized controlled trial (R-RCT) of LTOT prescribed 24 h/day compared with 15 h/day. The primary endpoint is all-cause-mortality at 1 year. Secondary endpoints include cause-specific mortality, hospitalizations, health-related quality of life, symptoms, and outcomes in interstitial lung disease. Methods/design Patients qualifying for LTOT are randomized to LTOT 24 h/day versus 15 h/day during 12 months using the Swedish Register for Respiratory Failure (Swedevox). Planned sample size in this pragmatic study is 2126 randomized patients. Clinical follow-up and concurrent treatments are according to routine clinical practice. Mortality, hospitalizations, and incident diseases are assessed using national Swedish registries with expected complete follow-up. Patient-reported outcomes are assessed using postal questionnaire at 3 and 12 months. Discussion The R-RCT approach combines the advantages of a prospective randomized trial and large clinical national registries for enrollment, allocation, and data collection, with the aim of improving the evidence-based use of LTOT. Trial registration Clinical Trial registered with www.clinicaltrials.gov, Title: REgistry-based Treatment Duration and Mortality in Long-term OXygen Therapy (REDOX); ID: NCT03441204.http://link.springer.com/article/10.1186/s12890-019-0809-7Register-based randomized controlled trialHypoxaemiaLong-term oxygen therapyOxygen durationChronic obstructive pulmonary diseaseInterstitial lung disease
collection DOAJ
language English
format Article
sources DOAJ
author Josefin Sundh
Anna Bornefalk-Hermansson
Zainab Ahmadi
Anders Blomberg
Christer Janson
David C. Currow
Christine F. McDonald
Nikki McCaffrey
Magnus Ekström
spellingShingle Josefin Sundh
Anna Bornefalk-Hermansson
Zainab Ahmadi
Anders Blomberg
Christer Janson
David C. Currow
Christine F. McDonald
Nikki McCaffrey
Magnus Ekström
REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocol
BMC Pulmonary Medicine
Register-based randomized controlled trial
Hypoxaemia
Long-term oxygen therapy
Oxygen duration
Chronic obstructive pulmonary disease
Interstitial lung disease
author_facet Josefin Sundh
Anna Bornefalk-Hermansson
Zainab Ahmadi
Anders Blomberg
Christer Janson
David C. Currow
Christine F. McDonald
Nikki McCaffrey
Magnus Ekström
author_sort Josefin Sundh
title REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocol
title_short REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocol
title_full REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocol
title_fullStr REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocol
title_full_unstemmed REgistry-based randomized controlled trial of treatment and Duration and mortality in long-term OXygen therapy (REDOX) study protocol
title_sort registry-based randomized controlled trial of treatment and duration and mortality in long-term oxygen therapy (redox) study protocol
publisher BMC
series BMC Pulmonary Medicine
issn 1471-2466
publishDate 2019-02-01
description Abstract Objective Long-term oxygen therapy (LTOT) during 15 h/day or more prolongs survival in patients with chronic obstructive pulmonary disease (COPD) and severe hypoxemia. No randomized controlled trial has evaluated the net effects (benefits or harms) from LTOT 24 h/day compared with 15 h/day or the effect in conditions other than COPD. We describe a multicenter, national, phase IV, non-superiority, registry-based, randomized controlled trial (R-RCT) of LTOT prescribed 24 h/day compared with 15 h/day. The primary endpoint is all-cause-mortality at 1 year. Secondary endpoints include cause-specific mortality, hospitalizations, health-related quality of life, symptoms, and outcomes in interstitial lung disease. Methods/design Patients qualifying for LTOT are randomized to LTOT 24 h/day versus 15 h/day during 12 months using the Swedish Register for Respiratory Failure (Swedevox). Planned sample size in this pragmatic study is 2126 randomized patients. Clinical follow-up and concurrent treatments are according to routine clinical practice. Mortality, hospitalizations, and incident diseases are assessed using national Swedish registries with expected complete follow-up. Patient-reported outcomes are assessed using postal questionnaire at 3 and 12 months. Discussion The R-RCT approach combines the advantages of a prospective randomized trial and large clinical national registries for enrollment, allocation, and data collection, with the aim of improving the evidence-based use of LTOT. Trial registration Clinical Trial registered with www.clinicaltrials.gov, Title: REgistry-based Treatment Duration and Mortality in Long-term OXygen Therapy (REDOX); ID: NCT03441204.
topic Register-based randomized controlled trial
Hypoxaemia
Long-term oxygen therapy
Oxygen duration
Chronic obstructive pulmonary disease
Interstitial lung disease
url http://link.springer.com/article/10.1186/s12890-019-0809-7
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