Rosa, Regis Goulart https://orcid.org/0000-0001-7881-9866
Cavalcanti, Alexandre Biasi
Azevedo, Luciano César Pontes
Veiga, Viviane Cordeiro
de Souza, Denise
dos Santos, Rosa da Rosa Minho
Schardosim, Raíne Fogliati de Carli
Rech, Gabriela Soares
Trott, Geraldine
Schneider, Daniel
Robinson, Caroline Cabral
Haubert, Tainá Aparecida
Pallaoro, Victoria Emanuele Lobo
Brognoli, Liége Gregoletto
de Souza, Ana Paula
Costa, Lauren Sezerá
Barroso, Bruna Machado
Pelliccioli, Melissa Pezzetti
Gonzaga, Janine
Studier, Nicole dos Santos
Dagnino, Ana Paula Aquistapase
Neto, Juliana de Mesquita
da Silva, Sabrina Souza
Gimenes, Bruna dos Passos
dos Santos, Vanessa Brzoskowski
Estivalete, Gabriel Pozza Muller
Pellegrino, Carolina de Moraes
Polanczyk, Carisi Anne
Kawano-Dourado, Letícia
Tomazini, Bruno Martins
Lisboa, Thiago Costa
Teixeira, Cassiano
Zampieri, Fernando Godinho
Zavascki, Alexandre Prehn
Gersh, Bernard J.
Avezum, Álvaro
Machado, Flávia Ribeiro
Berwanger, Otavio
Lopes, Renato Delascio
Falavigna, Maicon
Clinical trials referenced in this document:
Documents that mention this clinical trial
Association between acute disease severity and one-year quality of life among post-hospitalisation COVID-19 patients: Coalition VII prospective cohort study
https://doi.org/10.1007/s00134-022-06953-1
Funding for this research was provided by:
Pfizer (68065723)
Article History
Received: 30 August 2022
Accepted: 5 December 2022
First Online: 3 January 2023
Declarations
:
: RGR reports research grants from Pfizer related to this submitted work, and research grants from Pfizer and Brazilian Ministry of Health and lectures fees from Novartis outside of this submitted work. CAP declares research grants from National Institute for Health Technology Assessment, FAPERGS, CNPq, and Brazilian Ministry of Health (PROADI-SUS), and consultant and lecture fees from Novartis, Roche, Bayer, Bristol-Meyers-Squibb, Amgen, Pfizer, Astrazeneca outside of this submitted work. LKD reports research grants from Brazilian Ministry of Health (PROADI-SUS), Boehringer Ingelheim, Bristol-Myers-Squibb and consulting fees from Lilly, Roche and Gilead outside of this submitted work. FGZ reports research grants from Ionis Pharmaceuticals and Bactiguard and consultant from Bactiguard. APZ reports research grants from Pfizer and consultant from fees Spero Therapeutics outside of this submitted work. OB reports research grants from AstraZeneca, Pfizer, Bayer, Boehringer Ingelheim, Servier, and Amgen outside of this submitted work. RDL reports research grants from BMS, Glaxo Smith Kline, Medtronic, Portola, Bayer, Pfizer, Sanofi, Daiichi Sankyo, Merck and Boehringer Ingleheim, and consulting fees from Bayer, BMS, Glaxo Smith Kline, Portola, Merck, Boehringer Ingleheim, Daiichi Sankyo, Medtronic, Sanofi and Pfizer outside of this submitted work. The other authors have no conflict to declare.
: All five randomised clinical trials that compose the present cohort study, including their amendments for 1-year telephone follow-up, were approved by Brazil’s National Ethics Committee. Written informed consent was obtained from all participants or their proxies at the time of enrolment during hospital stay. Participants were re-consented during the first telephone call.
: Not applicable.
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