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Home Treatment of Older People with Symptomatic SARS-CoV-2 Infection (COVID-19): A structured Summary of a Study Protocol for a Multi-Arm Multi-Stage (MAMS) Randomized Trial to Evaluate the Efficacy and Tolerability of Several Experimental Treatments to Reduce the Risk of Hospitalisation or Death in outpatients aged 65 years or older (COVERAGE trial)

Authors :
Alexandre Duvignaud
Edouard Lhomme
Thierry Pistone
Racha Onaisi
Rémi Sitta
Valérie Journot
Duc Nguyen
Nathan Peiffer-Smadja
Antoine Crémer
Stéphane Bouchet
Thomas Darnaud
Delphine Poitrenaud
Lionel Piroth
Christine Binquet
Jean-François Michel
Benjamin Lefèvre
David Lebeaux
Josselin Lebel
Julie Dupouy
Caroline Roussillon
Anne Gimbert
Linda Wittkop
Rodolphe Thiébaut
Joanna Orne-Gliemann
Jean-Philippe Joseph
Laura Richert
Xavier Anglaret
Denis Malvy
the COVERAGE study group
Source :
Trials, Vol 21, Iss 1, Pp 1-3 (2020)
Publication Year :
2020
Publisher :
BMC, 2020.

Abstract

Abstract Objectives To assess the efficacy of several repurposed drugs to prevent hospitalisation or death in patients aged 65 or more with recent symptomatic SARS-CoV-2 infection (COVID-19) and no criteria for hospitalisation. Trial design Phase III, multi-arm (5) and multi-stage (MAMS), randomized, open-label controlled superiority trial. Participants will be randomly allocated 1:1:1:1:1 to the following strategies: Arm 1: Control arm Arms 2 to 5: Experimental treatment arms Planned interim analyses will be conducted at regular intervals. Their results will be reviewed by an Independent Data and Safety Monitoring Board. Experimental arms may be terminated for futility, efficacy or toxicity before the end of the trial. New experimental arms may be added if new evidence suggests that other treatments should be tested. A feasibility and acceptability substudy as well as an immunological substudy will be conducted alongside the trial. Participants Inclusion criteria are: 65-year-old or more; Positive test for SARS-CoV-2 on a nasopharyngeal swab; Symptoms onset within 3 days before diagnosis; No hospitalisation criteria; Signed informed consent; Health insurance. Exclusion criteria are: Inability to make an informed decision to participate (e.g.: dementia, guardianship); Rockwood Clinical Frailty Scale ≥7; Long QT syndrome; QTc interval > 500 ms; Heart rate 5.5 mmol/L or

Subjects

Subjects :
Medicine (General)
R5-920

Details

Language :
English
ISSN :
17456215
Volume :
21
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
edsdoj.f09c7f006a924356be2d7eab55c2380e
Document Type :
article
Full Text :
https://doi.org/10.1186/s13063-020-04619-1