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Comparison · NCT00445601-sae

Arm I: Gemcitabine vs Arm II: Placebo: serious adverse events

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. Arm I: Gemcitabine vs Arm II: Placebo: serious adverse events. Trial comparisons, record NCT00445601-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00445601-sae

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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 10.04240.02070.085wilson
Risk in group 20.02870.01230.0655wilson
Risk difference, group 1 minus group 20.0137-0.0290.0593newcombe hybrid score
Risk ratio, group 1 over group 21.480.4784.56log
Odds ratio, group 1 over group 21.50.4664.81log
Number needed to harm, for one more participant with a serious adverse event on Arm I: Gemcitabine than on Arm II: Placebo73.1from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Arm I: GemcitabinePatients receive intravesical gemcitabine hydrochloride over 1 hour post-TURBT.7165EG000
Group 2Arm II: PlaceboPatients receive intravesical placebo over 1 hour post-TURBT.5174EG001

Harm

What it counts
Total, serious adverse events
Time frame
Assessed every 3 months for 2 years, then every 6 months for 2 years

Source ClinicalTrials.gov

Trial

Title
S0337, Gemcitabine After Surgery in Treating Patients With Newly Diagnosed or Recurrent Bladder Cancer
NCT number
NCT00445601
Phases
PHASE3
Conditions
Bladder Cancer
Interventions
gemcitabine hydrochloride, placebo
Lead sponsor
SWOG Cancer Research Network
Results first posted
2018-04-24

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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