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

Sundh, Josefin, 1972- (författare)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Respiratory Medicine,Orebro Univ, Sch Med Sci, Dept Resp Med, Orebro, Sweden
Bornefalk-Hermansson, Anna, 1971- (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR)
Ahmadi, Zainab (författare)
Department of Clinical Sciences, Division of Respiratory Medicine & Allergology, Lund University, Lund, Sweden,Lund Univ, Div Resp Med & Allergol, Dept Clin Sci, Lund, Sweden
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Blomberg, Anders, 1961- (författare)
Umeå universitet,Avdelningen för medicin,Lungmedicin,Umea Univ, Div Med Resp Med, Dept Publ Hlth & Clin Med, Umea, Sweden
Janson, Christer (författare)
Uppsala universitet,Lung- allergi- och sömnforskning
Currow, David C. (författare)
Faculty of Health, University of Technology, Sydney, Australia,Univ Technol, Fac Hlth, Sydney, NSW, Australia
McDonald, Christine F. (författare)
Institute for Breathing and Sleep, Melbourne, Victoria, Australia,Inst Breathing & Sleep, Melbourne, Vic, Australia
McCaffrey, Nikki (författare)
Deakin Health Economics, Deakin University, Burwood, Victoria, Australia,Deakin Univ, Deakin Hlth Econ, Burwood, Vic, Australia
Ekström, Magnus (författare)
Department of Clinical Sciences, Division of Respiratory Medicine & Allergology, Lund University, Lund, Sweden,Lund Univ, Div Resp Med & Allergol, Dept Clin Sci, Lund, Sweden
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 (creator_code:org_t)
2019-02-26
2019
Engelska.
Ingår i: BMC Pulmonary Medicine. - : BioMed Central. - 1471-2466. ; 19:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • 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.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

Nyckelord

Chronic obstructive pulmonary disease
Health-related quality of life
Hospitalizations
Hypoxaemia
Interstitial lung disease
Long-term oxygen therapy
Mortality
Oxygen duration
Register-based randomized controlled trial
Symptoms

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