Synthetic CBD as a Therapy for COVID-19

  • STATUS
    Recruiting
  • days left to enroll
    30
  • participants needed
    50
  • sponsor
    Sheba Medical Center
Updated on 7 October 2021

Summary

The study aim to test proof of concept of CBD treatment for efficacy and safety in patients suffering with mild COVID-19 infection. The CBD will be delivered via oil droplets not containing THC, compared to placebo.

Details
Condition Cannabidiol, Carbidopa, COVID19
Treatment Placebo, CBD
Clinical Study IdentifierNCT04686539
SponsorSheba Medical Center
Last Modified on7 October 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

COVID 19 patients
Years and older

Exclusion Criteria

Respiratory failure requiring mechanical ventilation
Intensive care unit admission
Neutrophile con. < 1000 cells/mm3
Lymphocyte con < 500 cells/mm3
Liver enzymes 5 times higher then the norm
QT interval longer then 500 ms
Pregnancy
Hemodialysis renal replacement therapy
Active or prior psychotic event
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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