Comparison · NCT00967226-sae
Propranolol vs Prednisolone: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Propranolol vs Prednisolone: serious adverse events. Trial comparisons, record NCT00967226-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00967226-sae
On this page
Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0909 | 0.0162 | 0.377 | wilson | |
| Risk in group 2 | 0.625 | 0.306 | 0.863 | wilson | |
| Risk difference, group 1 minus group 2 | -0.534 | -0.784 | -0.105 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.145 | 0.0208 | 1.02 | log | |
| Odds ratio, group 1 over group 2 | 0.06 | 0.0049 | 0.735 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Propranolol than on Prednisolone | 1.87 | 1.28 | 9.51 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Propranolol | Assessing efficacy and tolerability of propranolol in management of symptomatic hemangiomas~propranolol: propranolol 0.5 mg/kg p.o. QID 6 months or less | 1 | 11 | EG000 |
| Group 2 | Prednisolone | Assessing efficacy and tolerability of prednisolone in management of symptomatic hemangiomas and comparing to propranolol.~Prednisolone: 1.0 mg/kg p.o. BID x 6 months or less | 5 | 8 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse events collected in first 9 months participants treated with medication.
Source ClinicalTrials.gov
Trial
- Title
- Propranolol Versus Prednisolone for Treatment of Symptomatic Hemangiomas
- NCT number
- NCT00967226
- Phases
- PHASE2
- Conditions
- Hemangioma of Infancy
- Interventions
- propranolol, Prednisolone
- Lead sponsor
- Nancy Bauman
- Results first posted
- 2016-02-24
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00967226?tab=results
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.
For software
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT00967226-sae