Last updated: February 21, 2021
Sponsor: Hamad Medical Corporation
Overall Status: Completed
Phase
N/A
Condition
N/ATreatment
N/AClinical Study ID
NCT04349592
MRC-05-001
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patient is in HMC facility for low-acuity, Covid-positive patients being quarantined.
- Positive Covid test on qualitative assay used during routine care (i.e. not as part ofQ-PROTECT)
- Age at least 18
Exclusion
Exclusion Criteria:
- Treating physician judges patient not appropriate for study participation for anyreason
- Age <18
- Breastfeeding or pregnancy (patient-reported pregnancy status is sufficient)
- Hypersensitivity to chloroquine or HC or AZ
- History of or known QT prolongation
- EKG required before study entry and on each visit during the subject's firstseven days on pro-tocol, during the time period HC is being taken
- Baseline QTc >480 if QRS width normal; QTc >510 if QRS >120
- Known G6PD deficiency, porphyria, or retinopathy (eye exam prior to study entry)
- Known hepatic or renal disease (or abnormality on liver or renal function testing atstudy day 1)
- Low magnesium or low potassium (by testing on day 1)
- Current (pre-study) therapy with antimalarial or dapsone
- Current (pre-study) therapy with antiviral agents (e.g. oseltamivir)
- Tisdale36 score exceeding 6 as tallied below (based on ACC recommendations)*
- 1 point each: age>67, female sex, or being on loop diuretic
- 2 points each: serum potassium <3.6, QTc>449, acute myocardial infarction
- 3 points each: sepsis, heart failure, QT-prolonging drugs
Study Design
Total Participants: 456
Study Start date:
April 14, 2020
Estimated Completion Date:
August 30, 2020
Study Description
Connect with a study center
Hamad Medical Corporation
Doha, 3050
QatarSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.