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

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

COVID-19 prophylaxis (excluding children) meta-analysis

Khera (inpatients) OBSangiotensin converting enzyme inhibitors (ACEIs)controlCOVID-19 prophylaxis (excluding children)serious
-/- inconclusive
    Khera (inpatients) OBSangiotensin receptor blockers (ARBs)controlCOVID-19 prophylaxis (excluding children)serious
    -/- inconclusive
      Khera (outpatients) OBSangiotensin converting enzyme inhibitors (ACEIs)controlCOVID-19 prophylaxis (excluding children)serious
      -/- inconclusive
        Khera (outpatients) OBSangiotensin receptor blockers (ARBs)controlCOVID-19 prophylaxis (excluding children)serious
        -/- inconclusive
          Morales OBSangiotensin converting enzyme inhibitors (ACEIs)controlCOVID-19 prophylaxis (excluding children)NA
          363785/248915 inconclusive
            Morales OBSangiotensin receptor blockers (ARBs)controlCOVID-19 prophylaxis (excluding children)NA
            363785/248915 inconclusive
              Morales OBSRenin-angiotensin-system-acting agentscontrolCOVID-19 prophylaxis (excluding children)NA
              363785/248915 inconclusive
                Reynolds (prophylaxis) OBSRenin-angiotensin-system-acting agentscontrolCOVID-19 prophylaxis (excluding children)serious
                -/- inconclusive
                  Mancia OBSangiotensin converting enzyme inhibitors (ACEIs)controlCOVID-19 prophylaxis (excluding children)serious
                  6272/30759 inconclusive
                    Mancia OBSangiotensin receptor blockers (ARBs)controlCOVID-19 prophylaxis (excluding children)serious
                    6272/30759 inconclusive

                      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).