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

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

preventing respiratory virus transmission meta-analysis

Barasheed RCTface maskcontrolpreventing respiratory virus transmissionNA
-/- suggested
  • suggested 59 % decrease in Influenza-like infection
Cowling
  NCT00425893		 RCTface maskcontrolpreventing respiratory virus transmissionNA
-/- inconclusive
    MacIntyre RCTface maskcontrolpreventing respiratory virus transmissionNA
    		-/- inconclusive
      Alfelali CRTface maskcontrolpreventing respiratory virus transmissionNA
      		-/- inconclusive
        MacIntyre CRTface maskcontrolpreventing respiratory virus transmissionNA
        		123/122 inconclusive
          Aiello
                      NCT00490633          		 CRTface maskcontrolpreventing respiratory virus transmissionNA
          		1623/1642 suggested
          • suggested 75 % decrease in Influenza-like infection
          Suess
                      NCT00833885          		 CRTface maskcontrolpreventing respiratory virus transmissionNA
          		26/30 suggested
          • suggested 68 % decrease in respiratory viral infections
          MacIntyre CRTface maskcontrolpreventing respiratory virus transmissionNA
          		-/- inconclusive
            Simmerman CRTface maskcontrolpreventing respiratory virus transmissionNA
            		-/- inconclusive
              Aiello
                              NCT00490633              		 CRTface maskcontrolpreventing respiratory virus transmissionNA
              		-/- inconclusive
                Canini
                                  NCT00774774                		 CRTface maskcontrolpreventing respiratory virus transmissionNA
                		52/53 inconclusive
                  Larson CRTface maskcontrolpreventing respiratory virus transmissionNA
                  		-/- 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).

                     

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