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Sci Rep ; 14(1): 19902, 2024 08 27.
Article in English | MEDLINE | ID: mdl-39191809

ABSTRACT

To evaluate the safety and the potential antiviral treatment of inhaled enriched heparin in patients with COVID-19. The specific objectives were to investigate the anticoagulation profile, antiviral and anti-inflammatory effects, and respiratory evolution of inhaled enriched heparin. We conducted a randomized, triple-blind, placebo-controlled Phase I/II clinical trial in hospitalized adults with COVID-19 receiving inhalation of enriched heparin or saline (placebo) every 4 h for 7 days. Among the 27 patients who completed the study, no changes in blood coagulation parameters were observed, indicating the safety of inhaled enriched heparin. The group receiving enriched heparin showed a significant reduction in the need for supplemental oxygen and improvement in respiratory parameters, such as the PaO2/FiO2 ratio. Inhalation of enriched heparin is shown to be safe and has also demonstrated potential therapeutic benefits for patients with COVID-19. These promising results justify the continuation of the study to the next phase, Phase II/III, to further evaluate the therapeutic efficacy of inhaled enriched heparin in the treatment of COVID-19-associated viral pneumonia.Trial registration: ClinicalTrials.gov. 08/02/2021. Identifier: NCT04743011.


Subject(s)
Anticoagulants , COVID-19 Drug Treatment , COVID-19 , Heparin , Humans , Heparin/administration & dosage , Male , Female , Middle Aged , Administration, Inhalation , Aged , COVID-19/virology , Anticoagulants/administration & dosage , Anticoagulants/therapeutic use , Nebulizers and Vaporizers , SARS-CoV-2 , Adult , Antiviral Agents/administration & dosage , Antiviral Agents/therapeutic use , Treatment Outcome
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