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Comparison · NCT01170117-sae

Olanzapine vs 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. Olanzapine vs Placebo: serious adverse events. Trial comparisons, record NCT01170117-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01170117-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 10.2130.1360.319wilson
Risk in group 20.1690.1010.268wilson
Risk difference, group 1 minus group 20.0445-0.08120.17newcombe hybrid score
Risk ratio, group 1 over group 21.260.6542.44log
Odds ratio, group 1 over group 21.340.5923.01log
Number needed to harm, for one more participant with a serious adverse event on Olanzapine than on Placebo22.5from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Olanzapine
Group receiving olanzapine~Olanzapine: Dosing of olanzapine will begin at 2.5 mg and will be titrated to a maximum dose of 10 mg. The target dose of 10 mg of olanzapine was selected because published data from studies that used this dose indicated that it was helpful to patients.
1675EG001
Group 2PlaceboControl group receiving placebo~Placebo: Control Group will receive placebo pill.1377EG000

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were collected during the 24 weeks of study participation (16 weeks of active participation, and 8 weeks of followup).

Source ClinicalTrials.gov

Trial

Title
Olanzapine Versus Placebo for Outpatients With Anorexia Nervosa
NCT number
NCT01170117
Phases
NA
Conditions
Anorexia Nervosa
Interventions
Olanzapine, Placebo
Lead sponsor
New York State Psychiatric Institute
Results first posted
2017-08-25

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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