Comparison · NCT01410448-sae
Immediate Everolimus (IE) vs Delayed Everolimus (DE): 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. Immediate Everolimus (IE) vs Delayed Everolimus (DE): serious adverse events. Trial comparisons, record NCT01410448-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01410448-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 | 0.378 | 0.313 | 0.448 | wilson | |
| Risk in group 2 | 0.321 | 0.259 | 0.39 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0572 | -0.0382 | 0.151 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.18 | 0.895 | 1.55 | log | |
| Odds ratio, group 1 over group 2 | 1.29 | 0.844 | 1.96 | log | |
| Number needed to harm, for one more participant with a serious adverse event on Immediate Everolimus (IE) than on Delayed Everolimus (DE) | 17.5 | 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 | Immediate Everolimus (IE) | Everolimus was started within 48 hours after graft reperfusion at a starting dose of 0.75 mg twice daily in combination with low-dose cyclosporine and steroids for 3 months. | 73 | 193 | EG000 |
| Group 2 | Delayed Everolimus (DE) | The standard dose of mycophenolate sodium was administered within 48 hours after graft reperfusion in combination with a full dose of cyclosporine and steroids. After28 +/- 4 days of treatment, mycophenolate sodium was discontinued and everolimus was introduced at a starting dose of 0.75 mg twice daily for 3 months. | 61 | 190 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Source ClinicalTrials.gov
Trial
- Title
- Everolimus in de Novo Kidney Transplant Recipients
- NCT number
- NCT01410448
- Phases
- PHASE3
- Conditions
- Kidney Transplantation
- Interventions
- Everolimus, Mycophenolate sodium, Cyclosporine, Steroids
- Lead sponsor
- Novartis Pharmaceuticals
- Results first posted
- 2017-06-16
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01410448?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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