Comparison · NCT00848250-sae
ACE Inhibitor vs No ACE Inhibitor: 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. ACE Inhibitor vs No ACE Inhibitor: serious adverse events. Trial comparisons, record NCT00848250-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00848250-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 | 0.364 | 0.152 | 0.646 | wilson | |
| Risk in group 2 | 0.222 | 0.0632 | 0.547 | wilson | |
| Risk difference, group 1 minus group 2 | 0.141 | -0.247 | 0.466 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.64 | 0.384 | 6.98 | log | |
| Odds ratio, group 1 over group 2 | 2 | 0.272 | 14.7 | log | |
| Number needed to harm, for one more participant with a serious adverse event on ACE Inhibitor than on No ACE Inhibitor | 7.07 | 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 | ACE Inhibitor | Patients already on an ACE inhibitor will continue it until the day of surgery~Angiotensin Converting Enzyme Inhibitor: Patients randomized to this group will continue their current dose of ACE inhibitors until surgery | 4 | 11 | EG000 |
| Group 2 | No ACE Inhibitor | Patients on ACE inhibitors who are randomized to stop their ACE inhibitor 48 hours prior to surgery~No ACE Inhibitor: Patients randomized to this group will stop their ACE inhibitors 48 hours before surgery | 2 | 9 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- From the start of surgery until hospital discharge, approximately 7 days
Source ClinicalTrials.gov
Trial
- Title
- Angiotensin Converting Enzyme Inhibitors During Cardiopulmonary Bypass in Infants and Children
- NCT number
- NCT00848250
- Phases
- NA
- Conditions
- Congenital Heart Disease
- Interventions
- Angiotensin Converting Enzyme Inhibitor, No ACE Inhibitor
- Lead sponsor
- Vanderbilt University Medical Center
- Results first posted
- 2017-07-26
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00848250?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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