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aTIV (Pooled) vs Licensed TIV: Number of Subjects Reporting Healthcare Utilization Across Vaccine Groups

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

Measures 6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.07860.07010.088wilsonClinicalTrials.gov
Risk in group 20.08250.07390.0921wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00393-0.01670.00884newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9520.8131.12logClinicalTrials.gov
Odds ratio, group 1 over group 20.9480.7981.13logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on aTIV (Pooled) than on Licensed TIV254from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1aTIV (Pooled)Subjects received one dose of MF59-adjuvanted trivalent subunit influenza vaccine (aTIV) from one of three consecutive lots (Lot 1, Lot 2 or Lot 3).2753,499OG000ClinicalTrials.gov
Group 2Licensed TIVSubjects received one dose of non-adjuvanted trivalent subunit influenza vaccine (TIV).2893,502OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Subjects Reporting Healthcare Utilization Across Vaccine GroupsClinicalTrials.gov
Description
The number of subjects with emergency room visits, unscheduled physician visits, and hospitalizations due to community acquired influenza or pneumonia, cardiopulmonary disease, cardiac disease, respiratory or pulmonary disease,in aTIV group compared to TIV group.
ClinicalTrials.gov
Time frameDay 1 through Day 366 post vaccinationClinicalTrials.gov
PopulationAnalysis was done on the mFAS (effectiveness).ClinicalTrials.gov

Trial 8

FieldValueSource
TitleSafety and Immunogenicity of MF59C.1 Adjuvanted Trivalent Subunit Influenza Vaccine in Elderly SubjectsClinicalTrials.gov
NCT numberNCT01162122ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsInfluenzaClinicalTrials.gov
InterventionsMF59 adjuvanted trivalent subunit influenza vaccine (aTIV), Non-adjuvanted trivalent subunit influenza vaccine (TIV)ClinicalTrials.gov
Lead sponsorNovartis VaccinesClinicalTrials.gov
Results first posted2014-06-12ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01162122?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.