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. 2021 Sep-Oct;47(5):e20210236. doi: 10.36416/1806-3756/e20210236

Table 1. Description of the studies included. (Continue...).

Study/country Participants (N) Type/identifier Context Eligibility criterion Group Outcome Follow-up period
Abella et al. 8
United States of America
132 Parallel RCT NCT04329923 Post-exposure prophylaxis Health care workers at COVID-19 units and no previous SARS-CoV-2 infection within the last 2 weeks Placebo
vs.
Hydroxychloroquine, 600 mg/day for 8 weeks
- Positive test for SARS-CoV-2 during 8 weeks
- Adverse events
8 weeks
Mitjà et al. 10
Spain
2,485 Cluster RCT NCT04304053 Post-exposure prophylaxis Health care workers, household contacts, and nursing home workers or residents with no previous SARS-CoV-2 infection within the last 2 weeks Usual care
vs.
Hydroxychloroquine, 800 mg on day 1, followed by 600 mg/day for 6 days
- Symptoms and positive test for SARS-CoV-2
- Hospitalization
- Adverse events
- Death
4 weeks
Boulware et al. 12
Unites States of America and Canada
821 Parallel RCT
NCT04308668
Post-exposure prophylaxis Household or occupational exposure to individuals with confirmed COVID-19 (distance ≤ 6 ft for >10 min with an infected subject or no use of face mask or eye shield) Placebo
vs.
Hydroxychloroquine, 800 mg on day 1 and 600 mg within 6-8 h after the first dose, followed by 600 mg/day for 4 days
- Positive test for SARS-CoV-2
- Hospitalization
- Adverse events
- Deaths
2 weeks
Rajasingham et al. 11
United States of America and Canada
1,483 Parallel RCT
NCT04328467
Pre-exposure prophylaxis Health care workers with high risk for SARS-CoV-2 exposure (ICU, ER, COVID-19 units) Placebo (folic acid)
vs.
Hydroxychloroquine, 400 mg on day 1 and 400 mg 6-8 h later, followed by 400 mg once a week for 12 weeks
vs.
Hydroxychloroquine, 400 mg on day 1 and 400 mg 6-8 h later, followed by 400 mg twice a week for 12 weeks
- COVID-19 free (no symptoms or negative RT-PCR result)
- Hospitalization
- Adverse events
- Death
12 weeks
Barnabas et al. 9
United States of America
689 Parallel RCT
NCT04328961
Post-exposure prophylaxis Contact with an index case diagnosed SARS-CoV-2 infection within 96 h Placebo
vs.
Hydroxychloroquine, 400 mg for 3 days, followed by 200 mg/day for 11 days
- Positive test for SARS-CoV-2
- Adverse events
14 days
Omrani et al. 14
Qatar
456 Triple parallel RCT
NCT04349592
Outpatients with mild COVID-19 Mild disease or no symptoms, outpatients Placebo
vs.
Hydroxychloroquine, 600 mg/day for 1 week
vs.
Hydroxychloroquine, 600 mg/day for 1 week + azithromycin
- Viral load
- Hospitalization
- Severe adverse events
- Death
14 days
Reis et al. 13
Brazil
685 Triple parallel RCT
NCT04403100
Mild COVID-19 Outpatients reporting less than 8 days since onset of flu-like symptoms or chest CT consistent with COVID-19 Placebo
vs.
Hydroxychloroquine, 800 mg as a loading dose, followed by 400 mg daily for 9 days
vs.
Lopinavir-ritonavir loading dose of 800 mg and 200 mg, respectively, every 12 h, followed by 400 mg and 100 mg, respectively, every 12 h for the following 9 days
- Adverse events
- Severe adverse events
- Hospitalization
- Deaths
90 days
Mitjà et al. 15
Spain
293 Parallel RCT
NCT04304053
Mild symptoms of COVID-19 Outpatients; symptoms for less than 5 days prior to enrollment Usual care
vs.
Hydroxychloroquine, 800 mg on day 1, followed by 400 mg/day for 6 days
- Viral load
- WHO progression scale
- Hospitalization
- Severe adverse events
- Deaths
28 days
Skipper et al. 16
United States of America and Canada
491 Parallel RCT
NCT04308668
Mild COVID-19 Outpatients, positive SARS-CoV-2 test and symptoms for ≤ 4 days or compatible symptoms after high-risk exposure to a contact with PCR-confirmed SARS-CoV-2 within the last 14 days Placebo
vs.
Hydroxychloroquine, 800 mg once and 600 mg in 6-8 h, followed by 600 mg daily for another 4 more days
- Hospitalization
- Adverse events
- Deaths
14 days

RCT: randomized controlled trial.