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Clinical Trial Summary

To measure the effect of Ivermectin (sub-cutaneous) with or without zinc 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.


Clinical Trial 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 demonstrate the antiviral effects of subcutaneous Ivermectin with or without zinc 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.. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04472585
Study type Interventional
Source Sheikh Zayed Federal Postgraduate Medical Institute
Contact Sohaib Ashraf, MBBS
Phone +923334474523
Email sohaib-ashraf@outlook.com
Status Recruiting
Phase Phase 1/Phase 2
Start date November 14, 2020
Completion date October 30, 2021

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