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Comparison · NCT00797277-sae

1. IM Olanzapine vs 2. IM Haloperidol Pus Lorazepam: 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. 1. IM Olanzapine vs 2. IM Haloperidol Pus Lorazepam: serious adverse events. Trial comparisons, record NCT00797277-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00797277-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 1000.0941wilson
Risk in group 2000.114wilson
Risk difference, group 1 minus group 20-0.1140.0941newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 11. IM OlanzapinePatients of this arm received 10 mg IM olanzapine after randomization037EG000
Group 22. IM Haloperidol Pus LorazepamPatients of this arm received 5 mg IM haloperidol plus 2 mg IM lorazepam after randomization030EG001

Harm

What it counts
Total, serious adverse events
Time frame
24 hours

Source ClinicalTrials.gov

Trial

Title
Intramuscular (IM) Olanzapine Versus IM Haloperidol Plus Lorazepam for Acute Agitation in Schizophrenia
NCT number
NCT00797277
Phases
PHASE3
Conditions
Schizophrenia, Schizoaffective Disorder, Agitation
Interventions
IM olanzapine, IM haloperidol plus lorazepam
Lead sponsor
National Taiwan University Hospital
Results first posted
2014-09-15

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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