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Comparison · NCT01363076-sae

Ketorolac Tromethamine (15 mg) vs Ketorolac Tromethamine (30 mg): 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. Ketorolac Tromethamine (15 mg) vs Ketorolac Tromethamine (30 mg): serious adverse events. Trial comparisons, record NCT01363076-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01363076-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 100.00000000000000005550.354wilson
Risk in group 20.07690.01370.333wilson
Risk difference, group 1 minus group 2-0.0769-0.3330.283newcombe 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 treat, for one fewer participant with a serious adverse event on Ketorolac Tromethamine (15 mg) than on Ketorolac Tromethamine (30 mg)13from 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 1Ketorolac Tromethamine (15 mg)Single intranasal (IN) dose of 15 mg ketorolac tromethamine for subjects weighing \<50 kg.07EG000
Group 2Ketorolac Tromethamine (30 mg)Single intranasal (IN) dose of 30 mg ketorolac tromethamine for subjects weighing ≥50 kg.113EG001

Harm

What it counts
Total, serious adverse events
Time frame
7 months

Source ClinicalTrials.gov

Trial

Title
The Pharmacokinetics of Ketorolac Tromethamine Administered Intranasally (IN) for Postoperative Pain in Children Aged 12 Through 17 Years
NCT number
NCT01363076
Phases
PHASE1
Conditions
Postoperative Pain
Interventions
Ketorolac Tromethamine, Ketorolac Tromethamine
Lead sponsor
Egalet Ltd
Results first posted
2012-04-09

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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