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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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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