Efficacy of Subcutaneous Ivermectin With or Without Zinc and Nigella Sativa in COVID-19 Patients
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- STATUS
- Recruiting
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- participants needed
- 40
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- sponsor
- Sohaib Ashraf
Summary
To measure the effect of Ivermectin (sub-cutaneous) with or without zinc and Nigella sativa in treating the COVID-19 patients to clear viral load of SARS-CoV-2 along with reduction in severity of symptoms and length of hospitalization of patients with COVID-19.
Description
This is a parallel assigned, randomized, controlled, multi-armed, investigator Initiated interventional study is designed to demonstrate efficacy to lower the viral load of COVID-19 and to demostrate the antiviral effects of subcutaneous Ivermection with or without zinc and Nigella sativa. in mild to moderate symptomatic patients who consent to randomization following a new diagnosis in Pakistan with COVID-19 (PCR positive). Investigators will follow up with participants daily and PCR will be done on alternate days in BSL-3 lab. Dose will only be repeated if test remained positive..
Details
| Condition | Coronavirus Infection, COVID, Sars-CoV2 |
|---|---|
| Age | 18years - 100years |
| Treatment | Placebo, zinc, Nigella Sativa / Black Cumin, Ivermectin Injectable Solution |
| Clinical Study Identifier | NCT04472585 |
| Sponsor | Sohaib Ashraf |
| Last Modified on | 19 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf 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.
Learn moreComplete 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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