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.