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Comparison · NCT01983683-deaths

Cadazolid vs Vancomycin: deaths from any cause

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

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Cadazolid vs Vancomycin: deaths from any cause. Trial comparisons, record NCT01983683-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01983683-deaths

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Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.03740.0210.0657wilson
Risk in group 20.04890.02980.079wilson
Risk difference, group 1 minus group 2-0.0114-0.04580.0227newcombe hybrid score
Risk ratio, group 1 over group 20.7660.3581.64log
Odds ratio, group 1 over group 20.7570.3421.68log
Number needed to treat, for one fewer death from any cause on Cadazolid than on Vancomycin87.4from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Cadazolidoral cadazolid 250 mg twice daily (bid) for 10 days11294EG000
Group 2Vancomycinoral vancomycin 125 mg 4 times per day (qid) for 10 days15307EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Serious and frequent adverse events are reported from study treatment initiation up to Day 17 on average (i.e., 7 days after end-of-treatment or study withdrawal) and all-cause mortality up to Day 40 on average (i.e. 28 to 32 days after end-of-treatment or study withdrawal)

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Cadazolid Versus Vancomycin in Subjects With Clostridium Difficile-associated Diarrhea
NCT number
NCT01983683
Phases
PHASE3
Conditions
Clostridium Difficile Infection
Interventions
Cadazolid, Vancomycin, Cadazolid-matching placebo, Vancomycin-matching placebo
Lead sponsor
Actelion
Results first posted
2018-04-13

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone 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.

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