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

COV-BARRIER
  NCT04421027		 RCTbaricitinibplaceboCOVID 19 hospitalizedlow
764/761 suggested
  • suggested 43 % decrease in deaths,deaths (time to event analysis only),death D28 with a high degree of certainty due to low risk of bias
  • inconclusive 12 % increase in clinical deterioration (PE) with a high degree of certainty due to low risk of bias
  • suggested 25 % increase in clinical improvement with a high degree of certainty due to low risk of bias
  • suggested 28 % increase in clinical improvement (14-day) with a high degree of certainty due to low risk of bias
ACTT-2 (Kalil)
  NCT04401579		 RCTbaricitinibplaceboCOVID 19 hospitalizedlow
515/518 conclusif
  • demonstrated 16 % increase in clinical improvement,clinical improvement (time to event analysis only) (PE) with a high degree of certainty due to low risk of bias
  • suggested 31 % decrease in death or ventilation with a high degree of certainty due to low risk of bias
  • suggested 36 % decrease in mechanical ventilation with a high degree of certainty due to low risk of bias

COVID 19 all comers meta-analysis

RECOVERY
  NCT04381936		 RCTbaricitinibstandard of careCOVID 19 all comerssome concern
4148/4008 conclusif
  • demonstrated 13 % decrease in deaths,death D28 (PE) with a moderate degree of certainty due to some concern in risk of bias
  • suggested 10 % decrease in death or ventilation with a moderate degree of certainty due to some concern in risk of bias

COVID-19 severe or critically meta-analysis

COV-BARRIER (critically ill)
  NCT04421027		 RCTbaricitinibplaceboCOVID-19 severe or criticallylow
51/50 suggested
  • suggested 46 % decrease in deaths,death D28 with a high degree of certainty due to low risk of bias
  • suggested 1.9-fold increase in clinical improvement with a high degree of certainty due to low risk of bias
3 studies excluded by filtering options (0 RCT / 3 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).

 

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