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Study Ref. Design studied treatmentcontrol treatmentpatientsstudy risk of biassample sizes Results

COVID-19 prophylaxis (excluding children) meta-analysis

Xia (66)
 
ChiCTR2000032459
RCTSinopharm Beijing (BBIBP-CorV)placeboCOVID-19 prophylaxis (excluding children)NA
-/- inconclusive
    No serious adverse event was reported within 28 days post vaccination
    1 study excluded by filtering options (0 RCT / 1 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).