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 hospitalized meta-analysis

Tolouian bromhexinestandard of careCOVID 19 hospitalizedhigh
59/52 no results
    Abdulamir
     
    NCT04753619
    RCTniclosamidestandard of careCOVID 19 hospitalizedsome concern
    75/75 inconclusive
      Ader (lopinavir/ritonavir plus interferon)
       
      NCT04315948
      RCTlopinavir/ritonavir plus interferon ß-1astandard of careCOVID 19 hospitalizedsome concern
      145/148 safety concern
      • statistically significant 30 % decrease in clinical improvement,clinical improvement (time to event analysis only) with a moderate degree of certainty due to some concern in risk of bias
      • statistically significant 86 % increase in serious adverse events with a moderate degree of certainty due to some concern in risk of bias
      • statistically significant 3.4-fold increase in arrhythmia with a moderate degree of certainty due to some concern in risk of bias
      • statistically significant 5.6-fold increase in elevated liver enzymes with a moderate degree of certainty due to some concern in risk of bias
      DisCoVeRy (remdesivir)
       
      NCT04315948
      RCTremdesivirstandard of careCOVID 19 hospitalizedsome concern
      429/428 no results
        Gaitan-Duarte (Rosuvastatin plus colchicine plus emtricitabine/tenofovir)
         
        NCT04359095
        RCTEmtricitabine/tenofovir plus colchicine plus rosuvastatinstandard of careCOVID 19 hospitalizedsome concern
        163/162 suggested
        • inconclusive 38 % decrease in deaths,death D28 (PE) with a moderate degree of certainty due to some concern in risk of bias
        • suggested 30 % decrease in mechanical ventilation with a moderate degree of certainty due to some concern in risk of bias
        Mahajan RCTremdesivirstandard of careCOVID 19 hospitalizedsome concern
        41/41 inconclusive
          Ansarin
           
          IRCT202003117046797N
          RCTbromhexinestandard of careCOVID 19 hospitalizedhigh
          39/39 suggested
          • inconclusive 91 % decrease in deaths (PE) but with a low degree of certainty due to high risk of bias
          • suggested 91 % decrease in mechanical ventilation (PE) but with a low degree of certainty due to high risk of bias
          • suggested 86 % decrease in ICU admission (PE) but with a low degree of certainty due to high risk of bias
          Duke university HCQ-AZI
           
          NCT04335552
          RCThydroxychloroquine plus macrolidesstandard of careCOVID 19 hospitalizedNA
          -/- inconclusive
            Lou Y
             
            ChiCTR2000029544
            RCTbaloxavir marboxilstandard of careCOVID 19 hospitalizedsome concern
            10/10 inconclusive
            • inconclusive 88 % decrease in viral clearance by day 14 (PE) with a moderate degree of certainty due to some concern in risk of bias
            RECOVERY
             
            NCT04381936
            RCTlopinavir/ritonavirstandard of careCOVID 19 hospitalizedsome concern
            1616/3424 inconclusive
            • inconclusive 3 % increase in deaths (PE) with a moderate degree of certainty due to some concern in risk of bias
            the trial Steering Committee concluded that there is no beneficial effect of lopinavir-ritonavir in patients hospitalised with COVID-19 and closed randomisation to that treatment arm
            RECOVERY (AZI, Horby)
             
            NCT04381936
            RCTazithromycinstandard of careCOVID 19 hospitalizedsome concern
            2582/5181 inconclusive
            • inconclusive 3 % decrease in deaths,deaths (time to event analysis only),death D28 (PE) with a moderate degree of certainty due to some concern in risk of bias
            Sadeghi
             
            IRCT20200128046294N2
            RCTsofosbuvir and daclatasvirstandard of careCOVID 19 hospitalizedsome concern
            35/35 suggested
            • suggested 2.6-fold increase in clinical improvement (14-day) (PE) with a moderate degree of certainty due to some concern in risk of bias
            Sekhavati
             
            IRCT20200415047092N1
            RCTazithromycinstandard of careCOVID 19 hospitalizedsome concern
            56/55 inconclusive
            • inconclusive 51 % decrease in deaths (PE) with a moderate degree of certainty due to some concern in risk of bias
            SOLIDARITY (lopi/rito)
             
            NCT04315948
            RCTlopinavir/ritonavirstandard of careCOVID 19 hospitalizedsome concern
            1399/1372 inconclusive
            • inconclusive 0 % increase in deaths (PE) with a moderate degree of certainty due to some concern in risk of bias
            SOLIDARITY (remdesivir)
             
            NCT04315948
            RCTremdesivirstandard of careCOVID 19 hospitalizedsome concern
            2750/2725 inconclusive
            • inconclusive 5 % decrease in deaths,deaths (time to event analysis only) (PE) with a moderate degree of certainty due to some concern in risk of bias
            Yakoot
             
            DRKS00022203
            RCTsofosbuvir and daclatasvirstandard of careCOVID 19 hospitalizedsome concern
            44/45 suggested
            • suggested 60 % increase in recovery (PE) with a moderate degree of certainty due to some concern in risk of bias

            COVID 19 all comers meta-analysis

            Norwegian NOR study (remdesivir)
             
            NCT04321616
            RCTremdesivirstandard of careCOVID 19 all comerssome concern
            43/58 no results
              ELACOI (Standard of care)
               
              NCT04252885
              RCTumifenovir (arbidol)standard of careCOVID 19 all comerssome concern
              16/7 inconclusive
                Jun C
                 
                NCT04252274
                RCTdarunavir cobicistatstandard of careCOVID 19 all comershigh
                15/15 inconclusive
                • inconclusive 42 % decrease in viral clearance by day 7 (PE) but with a low degree of certainty due to high risk of bias
                Lou (FAVIPIRAVIR)
                 
                ChiCTR2000029544
                RCTfavipiravir standard of careCOVID 19 all comerssome concern
                10/10 inconclusive
                • inconclusive 82 % decrease in viral clearance ,viral clearance by day 14 (PE) with a moderate degree of certainty due to some concern in risk of bias

                COVID-19 mild to moderate meta-analysis

                Bukhari
                 
                NCT04392713
                RCTivermectinstandard of careCOVID-19 mild to moderatehigh
                50/50 suggested
                • suggested 10.6-fold increase in viral clearance by day 7 but with a low degree of certainty due to high risk of bias
                FACCT Trial
                 
                NCT04392973
                RCTfavipiravir standard of careCOVID-19 mild to moderatesome concern
                125/129 inconclusive
                • inconclusive 15 % decrease in clinical improvement (time to event analysis only) (PE) with a moderate degree of certainty due to some concern in risk of bias
                Rashad A (AZI vs SoC) RCTazithromycinstandard of careCOVID-19 mild to moderatesome concern
                107/99 inconclusive
                  AVIFAVIR
                   
                  NCT04434248
                  RCTfavipiravir standard of careCOVID 19 hospitalized, COVID-19 mild to moderatesome concern
                  20/20 suggested
                  • suggested 2.9-fold increase in viral clearance ,viral clearance by day 7 (PE) with a moderate degree of certainty due to some concern in risk of bias
                  Adverse drug reactions to AVIFAVIR were reported in 7/40 (17.5%) patients, including diarrhea, nausea, vomiting, chest pain and an increase in liver transaminase levels. The adverse drug reactions were mild to moderate and caused early discontinuation of the study drug in 2/40 (5.0%) patients.
                  Chachar
                   
                  NCT04739410
                  RCTivermectinstandard of careCOVID-19 mild to moderatehigh
                  25/25 inconclusive
                  • inconclusive 19 % increase in clinical improvement,clinical improvement (7-day) (PE) but with a low degree of certainty due to high risk of bias
                  COALITION I Covid-19 Brazil (AZI, Cavalcanti)
                   
                  NCT04322123
                  RCTazithromycinstandard of careCOVID-19 mild to moderatesome concern
                  172/159 inconclusive
                  • inconclusive 18 % decrease in clinical improvement,clinical improvement (14-day) (PE) with a moderate degree of certainty due to some concern in risk of bias
                  Dabbous HM
                   
                  NCT04349241
                  RCTfavipiravir standard of careCOVID-19 mild to moderatesome concern
                  50/50 inconclusive
                    ELACOI (lopinavir/ritonavir)
                     
                    NCT04252885
                    RCTlopinavir/ritonavirstandard of careCOVID-19 mild to moderatesome concern
                    21/7 inconclusive
                      GS-US-540-5774, 10 days
                       
                      NCT04292730
                      RCTremdesivirstandard of careCOVID-19 mild to moderatesome concern
                      197/200 safety concern
                      • suggested 58 % increase in clinical improvement (14-day) with a moderate degree of certainty due to some concern in risk of bias
                      • suggested 88 % increase in clinical improvement (28-day) with a moderate degree of certainty due to some concern in risk of bias
                      • statistically significant 63 % increase in adverse events with a moderate degree of certainty due to some concern in risk of bias
                      The primary endpoint was not met, no odds ratio is reported because the proportional odds assumption was not met
                      GS-US-540-5774, 5 days
                       
                      NCT04292730
                      RCTremdesivirstandard of careCOVID-19 mild to moderatesome concern
                      199/200 conclusif
                      • demonstrated 65 % increase in clinical improvement (PE) with a moderate degree of certainty due to some concern in risk of bias
                      Khamis RCTfavipiravir plus interferonstandard of careCOVID-19 mild to moderatesome concern
                      44/45 inconclusive
                        Krolewiecki
                         
                        NCT004381884
                        RCTivermectinstandard of careCOVID-19 mild to moderatesome concern
                        30/15 inconclusive
                          Li T
                           
                          NCT04273763
                          RCTbromhexinestandard of careCOVID-19 mild to moderatesome concern
                          12/6 suggested
                          • inconclusive 52 % decrease in clinical deterioration (PE) with a moderate degree of certainty due to some concern in risk of bias
                          • suggested 9.0-fold increase in hospital discharge with a moderate degree of certainty due to some concern in risk of bias
                          NCT04542694
                           
                          NCT04542694
                          RCTfavipiravir standard of careCOVID-19 mild to moderatesome concern
                          100/100 suggested
                          • suggested 1.1-fold increase in clinical improvement,clinical improvement (7-day) (PE) with a moderate degree of certainty due to some concern in risk of bias
                          • suggested 12.0-fold increase in viral clearance with a moderate degree of certainty due to some concern in risk of bias
                          Ruzhentsova T
                           
                          NCT04501783
                          RCTfavipiravir standard of careCOVID-19 mild to moderatesome concern
                          112/56 suggested
                          • suggested 63 % increase in clinical improvement,clinical improvement (time to event analysis only) (PE) with a moderate degree of certainty due to some concern in risk of bias
                          • inconclusive 28 % increase in viral clearance ,viral clearance (time to event analysis only) (PE) with a moderate degree of certainty due to some concern in risk of bias
                          • suggested 28 % increase in clinical improvement (14-day) with a moderate degree of certainty due to some concern in risk of bias
                          • suggested 50 % increase in clinical improvement (7-day) with a moderate degree of certainty due to some concern in risk of bias
                          Shahbaznejad
                           
                          IRCT20111224008507N3
                          RCTivermectinstandard of careCOVID-19 mild to moderatesome concern
                          35/38 inconclusive
                            Udwadia
                             
                            CTRI/2020/05/025114
                            RCTfavipiravir standard of careCOVID 19 hospitalized, COVID-19 mild to moderatesome concern
                            75/75 safety concern
                            • inconclusive 37 % increase in viral clearance ,viral clearance (time to event analysis only) (PE) with a moderate degree of certainty due to some concern in risk of bias
                            • suggested 75 % increase in clinical improvement,clinical improvement (time to event analysis only),clinical improvement (28-day) with a moderate degree of certainty due to some concern in risk of bias
                            • suggested 94 % decrease in mechanical ventilation (time to event analysis only),mechanical ventilation with a moderate degree of certainty due to some concern in risk of bias
                            • statistically significant 5.4-fold increase in adverse events with a moderate degree of certainty due to some concern in risk of bias

                            COVID-19 severe or critically meta-analysis

                            Cao
                             
                            ChiCTR2000029308
                            RCTlopinavir/ritonavirstandard of careCOVID-19 severe or criticallysome concern
                            99/100 suggested
                            • inconclusive 31 % increase in clinical improvement,clinical improvement (time to event analysis only) (PE) with a moderate degree of certainty due to some concern in risk of bias
                            • suggested 94 % increase in clinical improvement (14-day) with a moderate degree of certainty due to some concern in risk of bias
                            COALITION II Covid-19 Brazil (Furtado)
                             
                            NCT04321278
                            RCTazithromycinstandard of careCOVID-19 severe or criticallysome concern
                            214/183 safety concern
                            • inconclusive 26 % decrease in clinical improvement,clinical improvement (14-day) (PE) with a moderate degree of certainty due to some concern in risk of bias
                            • statistically significant 6 % decrease in clinical improvement (7-day) with a moderate degree of certainty due to some concern in risk of bias
                            REMAP-CAP (lopinavir/ritonavir only)
                             
                            NCT02735707
                            RCTlopinavir/ritonavirstandard of careCOVID-19 severe or criticallysome concern
                            268/377 safety concern
                            • statistically significant 17 % decrease in hospital discharge with a moderate degree of certainty due to some concern in risk of bias
                            REMAP-CAP (lopinavir/ritonavir plus hydroxychloroquine)
                             
                            NCT02735707
                            RCTLopinavir/ritonavir plus hydroxychloroquinestandard of careCOVID-19 severe or criticallysome concern
                            29/377 safety concern
                            • suggested 42 % decrease in deaths,deaths (time to event analysis only) with a moderate degree of certainty due to some concern in risk of bias
                            • statistically significant 37 % decrease in hospital discharge with a moderate degree of certainty due to some concern in risk of bias
                            6 studies excluded by filtering options (0 RCT / 6 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).