Status:
UNKNOWN
Clinical Study Designed to Evaluate the Effect of CimetrA in Patients Diagnosed With COVID-19
Lead Sponsor:
MGC Pharmaceuticals d.o.o
Conditions:
Corona Virus Infection
Covid19
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
A preparation of CimertrA, comprising Artemisinin, Curcumin, and Boswellia, and Vitamin C in a nanoparticular formulation, is proposed as a treatment for the disease associated with the novel coronavi...
Detailed Description
The study will take place during the patient's hospitalization due to a COVID-19 infection. The study will last up to 4 weeks, until the conclusion on day 28. In case of hospital discharge within the ...
Eligibility Criteria
Inclusion
- Confirmed SARS-CoV-2 infection (according to nationally authorized laboratory criteria)
- Hospitalized patient with COVID-19 of moderate stable or worsening severity not requiring ICU admission.
- Age: 18 years old and above.
- Subjects must be under observation or admitted to a controlled facility or hospital (home quarantine is not sufficient).
- Ability to receive treatment by spray into the oral cavity
Exclusion
- Tube feeding or parenteral nutrition.
- Patients with scores 5 or above per the Ordinal Scale for Clinical Improvement published by the WHO. (i.e., who need oxygen supply beyond use of nozzles or simple mask)
- Need for admission to ICU during the present hospitalization at any time prior to completion of the recruitment to the study.
- Any condition which, in the opinion of the Principal Investigator, would prevent full participation in this trial or would interfere with the evaluation of the trial endpoints.
Key Trial Info
Start Date :
June 11 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2023
Estimated Enrollment :
252 Patients enrolled
Trial Details
Trial ID
NCT04802382
Start Date
June 11 2021
End Date
April 1 2023
Last Update
August 24 2022
Active Locations (2)
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1
Nazareth Hospital EMMS
Nazareth, North, Israel
2
Rambam Medical Center
Haifa, Israel