Overview

Effectiveness of Ivermectin in SARS-CoV-2/COVID-19 Patients

Status:
Completed
Trial end date:
2020-06-30
Target enrollment:
0
Participant gender:
All
Summary
Background: The first case of Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) were diagnosed in Wuhan, China in 2019. In the first half of 2020 this disease has already converted into a global pandemic. Objectives: To assess the efficacy of Ivermectin in mild cases of COVID-19 patients on the basis of predefined assessment criteria. Study Settings: Fatima Memorial Hospital, Lahore Study Design: Open label randomized control trial. Duration of Study: From 1st May, 2020 to 30th June, 2020.Patients & Methods: Sample size and technique: Sample size was 50 patients; 25 patients were kept in control group and 25 patients were kept in experimental group
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
FMH College of Medicine and Dentistry
Treatments:
Ivermectin
Criteria
Inclusion Criteria:

- All patients diagnosed with COVID-19 infection with positive reverse transcriptase
RT-PCR test, who were willing to participate in this study

- Patients having age of 18-75 years

- Patients of both genders male and female

- Patients who had mild symptoms of Corona virus disease and RT- PCR positive for
SARS-Cov-2

- Ability to take oral medication and were willing to adhere to the drug intake regimen

Exclusion Criteria:

- Known severe allergic reactions to Ivermectin

- Pregnancy or breastfeeding

- Severe symptoms likely attributed to Cytokine Release Storm

- Malignant diseases

- Chronic kidney disease

- Cirrhosis liver with Child class B or C