Comparison · NCT01490580-sae
Atropine + Propofol vs Atropine + Atracurium + Sufentanil: 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. Atropine + Propofol vs Atropine + Atracurium + Sufentanil: serious adverse events. Trial comparisons, record NCT01490580-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01490580-sae
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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 | 0.108 | 0.0581 | 0.193 | wilson | |
| Risk in group 2 | 0.2 | 0.127 | 0.3 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0916 | -0.204 | 0.0204 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.542 | 0.254 | 1.16 | log | |
| Odds ratio, group 1 over group 2 | 0.486 | 0.201 | 1.18 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Atropine + Propofol than on Atropine + Atracurium + Sufentanil | 10.9 | from the risk difference interval | the interval includes no difference |
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 | Atropine + Propofol | atropine+ propofol: Atropine bolus: 20 µg/kg Propofol injected over 60 seconds: 1 mg/kg for infants \< 1000g - Renewable once 2.5 mg/kg for infants \> 1000G - Possible additional dose of 1 mg/kg | 9 | 83 | EG000 |
| Group 2 | Atropine + Atracurium + Sufentanil | atropine + atracurium + sufentanil: Atropine bolus: 20 µg/kg Atracurium: 0.3 mg/kg- Possible additional dose of 0.1 mg/kg Sufentanil: 0.1 µg/kg for infants \< 1000g 0.2 µg/kg for infants \> 1000g | 16 | 80 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Source ClinicalTrials.gov
Trial
- Title
- Premedication Trial for Tracheal Intubation of the NEOnate
- NCT number
- NCT01490580
- Phases
- PHASE2, PHASE3
- Conditions
- Premedication, Endotracheal Intubation
- Interventions
- atropine+ propofol, atropine + atracurium + sufentanil
- Lead sponsor
- Centre Hospitalier Intercommunal Creteil
- Results first posted
- 2019-09-13
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01490580?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.
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