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Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial

INTRODUCTION: The COVID-19 pandemic caused by the virus SARS-CoV has spread rapidly and caused damage worldwide. Data suggest a major overrepresentation of hypertension and diabetes among patients experiencing severe courses of COVID-19 including COVID-19-related deaths. Many of these patients recei...

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Autores principales: Kliim-Hansen, Vivian, Gasbjerg, Lærke Smidt, Ellegaard, Anne-Marie, Lorentsson, Hans Johan Niklas, Lynggaard, Mads Bank, Hagemann, Christoffer Andersen, Legart, Christian, Mathiesen, David Siersbæk, Sivapalan, Pradeesh, Jensen, Jens-Ulrik Stæhr, Vilsbøll, Tina, Christensen, Mikkel Bring, Knop, Filip Krag
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716414/
https://www.ncbi.nlm.nih.gov/pubmed/36450422
http://dx.doi.org/10.1136/bmjopen-2022-062895
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author Kliim-Hansen, Vivian
Gasbjerg, Lærke Smidt
Ellegaard, Anne-Marie
Lorentsson, Hans Johan Niklas
Lynggaard, Mads Bank
Hagemann, Christoffer Andersen
Legart, Christian
Mathiesen, David Siersbæk
Sivapalan, Pradeesh
Jensen, Jens-Ulrik Stæhr
Vilsbøll, Tina
Christensen, Mikkel Bring
Knop, Filip Krag
author_facet Kliim-Hansen, Vivian
Gasbjerg, Lærke Smidt
Ellegaard, Anne-Marie
Lorentsson, Hans Johan Niklas
Lynggaard, Mads Bank
Hagemann, Christoffer Andersen
Legart, Christian
Mathiesen, David Siersbæk
Sivapalan, Pradeesh
Jensen, Jens-Ulrik Stæhr
Vilsbøll, Tina
Christensen, Mikkel Bring
Knop, Filip Krag
author_sort Kliim-Hansen, Vivian
collection PubMed
description INTRODUCTION: The COVID-19 pandemic caused by the virus SARS-CoV has spread rapidly and caused damage worldwide. Data suggest a major overrepresentation of hypertension and diabetes among patients experiencing severe courses of COVID-19 including COVID-19-related deaths. Many of these patients receive renin-angiotensin system (RAS) inhibiting therapy, and evidence suggests that treatment with angiotensin II receptor blockers (ARBs) could attenuate SARS-CoV-induced acute respiratory distress syndrome, and ACE inhibitors and ARBs have been suggested to alleviate COVID-19 pulmonary manifestations. This randomised clinical trial will address whether RAS inhibiting therapy should be continued or discontinued in hospitalised patients with COVID-19. METHODS AND ANALYSIS: This trial is a 30-day randomised parallel-group non-inferiority clinical trial with an embedded mechanistic substudy. In the main trial, 215 patients treated with a RAS inhibitor will be included. The participants will be randomly assigned in a 1:1 ratio to either discontinue or continue their RAS inhibiting therapy in addition to standard care. The patients are included during hospitalisation and followed for a period of 30 days. The primary end point is number of days alive and out of hospital within 14 days after recruitment. In a mechanistic substudy, 40 patients treated with RAS inhibition, who are not in hospital and not infected with COVID-19 will be randomly assigned to discontinue or continue their RAS inhibiting therapy with the primary end point of serum ACE2 activity. ETHICS AND DISSEMINATION: This trial has been approved by the Scientific-Ethical Committee of the Capital Region of Denmark (identification no. H-20026484), the Danish Medicines Agency (identification no. 2020040883) and by the Danish Data Protection Agency (P-2020-366). The results of this project will be compiled into one or more manuscripts for publication in international peer-reviewed scientific journals. TRIAL REGISTRATION NUMBER: 2020-001544-26; NCT04351581.
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spelling pubmed-97164142022-12-03 Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial Kliim-Hansen, Vivian Gasbjerg, Lærke Smidt Ellegaard, Anne-Marie Lorentsson, Hans Johan Niklas Lynggaard, Mads Bank Hagemann, Christoffer Andersen Legart, Christian Mathiesen, David Siersbæk Sivapalan, Pradeesh Jensen, Jens-Ulrik Stæhr Vilsbøll, Tina Christensen, Mikkel Bring Knop, Filip Krag BMJ Open Infectious Diseases INTRODUCTION: The COVID-19 pandemic caused by the virus SARS-CoV has spread rapidly and caused damage worldwide. Data suggest a major overrepresentation of hypertension and diabetes among patients experiencing severe courses of COVID-19 including COVID-19-related deaths. Many of these patients receive renin-angiotensin system (RAS) inhibiting therapy, and evidence suggests that treatment with angiotensin II receptor blockers (ARBs) could attenuate SARS-CoV-induced acute respiratory distress syndrome, and ACE inhibitors and ARBs have been suggested to alleviate COVID-19 pulmonary manifestations. This randomised clinical trial will address whether RAS inhibiting therapy should be continued or discontinued in hospitalised patients with COVID-19. METHODS AND ANALYSIS: This trial is a 30-day randomised parallel-group non-inferiority clinical trial with an embedded mechanistic substudy. In the main trial, 215 patients treated with a RAS inhibitor will be included. The participants will be randomly assigned in a 1:1 ratio to either discontinue or continue their RAS inhibiting therapy in addition to standard care. The patients are included during hospitalisation and followed for a period of 30 days. The primary end point is number of days alive and out of hospital within 14 days after recruitment. In a mechanistic substudy, 40 patients treated with RAS inhibition, who are not in hospital and not infected with COVID-19 will be randomly assigned to discontinue or continue their RAS inhibiting therapy with the primary end point of serum ACE2 activity. ETHICS AND DISSEMINATION: This trial has been approved by the Scientific-Ethical Committee of the Capital Region of Denmark (identification no. H-20026484), the Danish Medicines Agency (identification no. 2020040883) and by the Danish Data Protection Agency (P-2020-366). The results of this project will be compiled into one or more manuscripts for publication in international peer-reviewed scientific journals. TRIAL REGISTRATION NUMBER: 2020-001544-26; NCT04351581. BMJ Publishing Group 2022-11-30 /pmc/articles/PMC9716414/ /pubmed/36450422 http://dx.doi.org/10.1136/bmjopen-2022-062895 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Infectious Diseases
Kliim-Hansen, Vivian
Gasbjerg, Lærke Smidt
Ellegaard, Anne-Marie
Lorentsson, Hans Johan Niklas
Lynggaard, Mads Bank
Hagemann, Christoffer Andersen
Legart, Christian
Mathiesen, David Siersbæk
Sivapalan, Pradeesh
Jensen, Jens-Ulrik Stæhr
Vilsbøll, Tina
Christensen, Mikkel Bring
Knop, Filip Krag
Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial
title Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial
title_full Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial
title_fullStr Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial
title_full_unstemmed Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial
title_short Protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without COVID-19: the RASCOVID-19 trial
title_sort protocol for a 30-day randomised, parallel-group, non-inferiority, controlled trial investigating the effects of discontinuing renin-angiotensin system inhibitors in patients with and without covid-19: the rascovid-19 trial
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716414/
https://www.ncbi.nlm.nih.gov/pubmed/36450422
http://dx.doi.org/10.1136/bmjopen-2022-062895
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