COVID Clinical Trial
Official title:
To Study the Effectiveness of Ivermectin With Standard of Care Treatment Versus Standard of Care Treatment for COVID 19 Cases. A Pilot Study
At present, there are no specific treatments for COVID-19. WHO recommends four treatments for COVID 19 with drugs i.eRemdesivir, Lopinavir/ ritonavir, Lopinavir/ ritonavir with interferon beta -1a, and chloroquine or hydroxychloroquine. Currently, there are several ongoing clinical trials evaluating potential treatments. Recently, LeonCaly reported that Ivermectin, an FDA-approved anti-parasitic previously shown to have broad-spectrum anti-viral activity in vitro, is an inhibitor of the causative virus (SARS-CoV-2), with a single addition to Vero-hSLAM cells 2 hours post infection with SARSCoV-2 able to effect about 5000-fold reduction in viral RNA at 48 h. Ivermectin therefore warrant further investigation for possible benefits in humans. The study rationale is to understand the effect of the drug on eradication of virus.
This study aims to confirm the antivirus effectiveness of Ivermectin on coronavirus i.e COVID
19 then to explore its potential use in the combating to the COVID 19 pandemics.
Enrollment of subject into the trial shall only occur after providing written permission to
voluntarily participate into the study by signing and dating the informed consent form before
starting any trial related treatment. 50 cases of COVID-19 will be enrolled into the trial.
The trial shall be divided into two groups. First group with 25 confirmed cases of COVID 19
shall be treated with Ivermectin 200 to 400 mcg per kg body weight on day 1 and day 2 along
with standard treatment of the hospital protocol. The second group with 25 confirmed cases of
COVID 19 shall be treated with standard treatment as per hospital protocol for COVID 19.
Subjects in both the arms shall be followed up for recovery of death with regular monitoring
as per below schedule.
1. Test for virus at 1, 3 & 5 days from beginning of trial drug started for the patient in
the hospital
2. Clinical profile of the patient every day of hospitalization
3. Investigation of pulmonary function and oxygen saturation every day of hospitalization
4. The day a patient is put on ventilator and the day when removed
5. The day a patient develops acute respiratory distress syndrome and the day when relieved
All the above data shall be collected on paper case record form for interim and final
analysis from start of the trial i.e enrollment, treatment and follow-up. Viral test to
monitor the eradication of Virus shall be done free of cost from third day of enrollment
and providing the study drug on daily basis upto eradication of virus or completion of
the trial
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