Study explorer (study characteristics and results) method abbreviations pdf   xlsx

display ongoing studies
Study Ref. Design studied treatmentcontrol treatmentpatientsstudy risk of biassample sizes Results deaths Eviral clearance Ehospitalization or death E

COVID-19 prophylaxis (excluding children) meta-analysis

EPICOS (Polo) RCThydroxychloroquineplaceboCOVID-19 prophylaxis (excluding children)some concern
231/223 inconclusive
HERO-HCQ (Naggie)
 
NCT04334148
RCThydroxychloroquineplaceboCOVID-19 prophylaxis (excluding children)some concern
683/676 inconclusive
Rojas-Serrano
 
NCT04318015
RCThydroxychloroquineplaceboCOVID-19 prophylaxis (excluding children)some concern
65/65 inconclusive
Barnabas RV
 
NCT04328961
RCThydroxychloroquineplaceboCOVID-19 prophylaxis (excluding children)low
407/422 safety concern
BCN PEP-CoV-2-Study 1 (Mitja NEJM)
 
NCT04304053
RCThydroxychloroquinestandard of careCOVID-19 prophylaxis (excluding children)some concern
1116/1198 safety concern -29%
COVID PREP HCQ (2x week, Rajasingham)
 
NCT04328467
RCThydroxychloroquineplaceboCOVID-19 prophylaxis (excluding children)low
495/494 safety concern
COVID-PEP-Post exposure (Boulware)
 
NCT04308668
RCThydroxychloroquineplaceboCOVID-19 prophylaxis (excluding children)low
414/407 safety concern -2%
PATCH-cohort 3 PreP (Abella)
 
NCT04329923
RCThydroxychloroquineplaceboCOVID-19 prophylaxis (excluding children)some concern
66/66 inconclusive 0%
6 studies excluded by filtering options (4 RCT / 2 OBS)

PE: primary endpoint; (a): to be demonstrated a result must be statistically significant on a primary endpoint (with multiplicity adjustment if necessary);
Study risk of bias assessed for the study primary endpoint(s) or the main endpoints in case of no formally defined primary endpoint(s).