Comparative Study of Hydroxychloroquine and Ivermectin in COVID-19 Prophylaxis
Coronavirus Infections
About this trial
This is an interventional prevention trial for Coronavirus Infections focused on measuring Coronavirus Infections, Health Personnel, Hydroxychloroquine, Pre-Exposure Prophylaxis, Antimalarials, Antirheumatic Agents, Ivermectin
Eligibility Criteria
Inclusion Criteria:
- Aged 18 - 70 years;
- Professionals working in areas of high exposure and high risk of transmission of SARS-COV-2;
- Understands and agrees to comply with planned study procedures;
- Signed informed consent for participation in the study.
Exclusion Criteria:
- Pregnancy or breastfeeding;
- Major allergy to Hidroxychloroquine, chloroquine or 4-aminoquinolines;
- Serum potassium lower than 3.4 mEq/l;
- Serum magnesium lower than 1.7 mg/dL;
- QTc interval > 470 ms for man and > 480 ms for woman;
- Weight < 40 kg;
Sites / Locations
- Drug Research and Development Center (NPDM), Federal University of Ceará (UFC)Recruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Hydroxychloroquine
Ivermectin
Oral hydroxychloroquine 400 mg twice a day on day 1, one 400 mg tablet on day 2, 3, 4, and 5, followed by one 400 mg tablets every 05 days until day 50th associated with with 20 milligrams twice on day of active zinc for 45 consecutive days
Oral ivermectin dosage guidelines based on participant body weight, once on day for 2 consecutive days. This dose schedule should be repeated every 14 days for 45 days associated with 20 milligrams twice on day of active zinc.