Multicenter Randomized Trial of Methylprednisolone vs. Intravenous Immunoglobulins to Treat the Pediatric Inflammatory Multisystem Syndrome-Temporally Associated With SARS-CoV-2 (PIMS-TS): Protocol of the Swissped RECOVERY Trial.

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License: CC BY 4.0
Serval ID
serval:BIB_E481C0B06A00
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Multicenter Randomized Trial of Methylprednisolone vs. Intravenous Immunoglobulins to Treat the Pediatric Inflammatory Multisystem Syndrome-Temporally Associated With SARS-CoV-2 (PIMS-TS): Protocol of the Swissped RECOVERY Trial.
Journal
Frontiers in pediatrics
Author(s)
Welzel T., Schöbi N., André M.C., Bailey DGN, Blanchard-Rohner G., Buettcher M., Grazioli S., Koehler H., Perez M.H., Trück J., Vanoni F., Zimmermann P., Atkinson A., Sanchez C., Whittaker E., Faust S.N., Bielicki J.A., Schlapbach L.J.
Working group(s)
Swissped Recovery Trial
ISSN
2296-2360 (Print)
ISSN-L
2296-2360
Publication state
Published
Issued date
2022
Peer-reviewed
Oui
Volume
10
Pages
905046
Language
english
Notes
Publication types: Journal Article
Publication Status: epublish
Abstract
In 2020, a new disease entitled Pediatric Inflammatory Multisystem Syndrome temporally associated with COVID-19 (PIMS-TS), or Multisystem Inflammatory Syndrome in Children (MIS-C), emerged, with thousands of children affected globally. There is no available evidence based on randomized controlled trials (RCT) to date on the two most commonly used immunomodulatory treatments, intravenous immunoglobulins (IVIG) and corticosteroids. Therefore, the Swissped RECOVERY trial was conducted to assess whether intravenous (IV) methylprednisolone shortens hospital length of stay compared with IVIG.
Swissped RECOVERY is an ongoing investigator-initiated, open-label, multicenter two-arm RCT in children and adolescents <18 years hospitalized with a diagnosis of PIMS-TS. The trial is recruiting at 10 sites across Switzerland. Patients diagnosed with PIMS-TS are randomized 1:1 to methylprednisolone IV (10 mg/kg/day for 3 days) or IVIG (2 g/kg as a single dose). The primary outcome is hospital length of stay censored at day 28, death, or discharge (whichever is first). The target total sample size is ~80 patients 1:1 randomized to each study arm. Ancillary and exploratory studies on inflammation, vaccination acceptance and coverage, long-term outcomes, and healthcare costs are pre-planned.
Currently, robust trial evidence for the treatment of PIMS-TS is lacking, with a controversy surrounding the use of corticosteroids vs. IVIG. This trial will provide evidence for the effectiveness and safety of these two treatments.
The study protocol, which was designed based on the U.K. RECOVERY trial, the patient information and consent forms, and other study-specific study documents were approved by the local ethics committees (Project ID: 2021-00362).
The study is registered on the Swiss National Clinical Trials Portal (SNCTP000004720) and Clinicaltrials.gov (NCT04826588).
Keywords
COVID-19, MIS-C, SARS-CoV-2, children, mortality, quality of life, treatment, trial
Pubmed
Web of science
Open Access
Yes
Create date
17/06/2022 17:51
Last modification date
27/06/2022 5:39
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