| Grant number: | 20/12110-9 |
| Support Opportunities: | Research Grants - Research in Public Policies |
| Start date: | March 01, 2021 |
| End date: | February 28, 2023 |
| Field of knowledge: | Health Sciences - Medicine - Psychiatry |
| Agreement: | CNPq - PPSUS |
| Principal Investigator: | José Alexandre de Souza Crippa |
| Grantee: | José Alexandre de Souza Crippa |
| Host Institution: | Faculdade de Medicina de Ribeirão Preto (FMRP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil |
| City of the host institution: | Ribeirão Preto |
| Associated researchers: | Alline Cristina de Campos ; Antonio Waldo Zuardi ; Flávia de Lima Osório ; Francisco Silveira Guimaraes ; Jaime Eduardo Cecilio Hallak |
Abstract
The aim of this work is to conduct a randomized, double-blind, placebo-controlled clinical trial to assess the efficacy and safety of cannabidiol (CBD - 300 mg a day) in patients infected with SARS-CoV-2. The specific objectives are to assess whether, in patients with mild and moderate forms of SARS-CoV-2, daily use of CBD 300 mg for fourteen days is capable of: i) decrease viral load; ii) modify inflammatory parameters, such as cytokines, measured from serum; iii) reduceclinical and emotional symptoms through daily clinical evaluation; iv) improve the quality of life and sleep; v) reduce hospitalization and worsen the severity of the disease; v) Monitor the possible adverse effects of CBD use in these patients vi) Evaluate whether CBD 300 mg can prevent depression, burnout, PTSD and other neuropsychiatric disorders in SARS-CoV-2 patients; vii) Evaluate if CBD can prevent central structural and functional abnormalities in SARS-CoV-2 patients as assessed by DTI diffusion tensor imaging and rsfMRI - resting-state functional magnetic resonance imaging. (AU)
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