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 Ehospitalization Econfirmed COVID (any severity) E

COVID-19 prophylaxis (excluding children) meta-analysis

Accorsi OBSfirst booster dosecontrolCOVID-19 prophylaxis (excluding children)NA
-/- no results
Mattiuzzi OBSfirst booster dosecontrolCOVID-19 prophylaxis (excluding children)NA
-/- suggested -88% -76% -76%
Ontario (Buchan) OBSfirst booster dosecontrolCOVID-19 prophylaxis (excluding children)NA
-/- suggested -33%
Tenforde OBSfirst booster dosecontrolCOVID-19 prophylaxis (excluding children)NA
-/- suggested -87%
England (Andrews) OBSfirst booster dosecontrolCOVID-19 prophylaxis (excluding children)NA
581/130867 suggested -68%
Sisonke 2 (booster)
 
NCT05148845
OBSfirst booster dosecontrolCOVID-19 prophylaxis (excluding children)NA
-/- suggested -76%

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).