Comparison · NCT00661037-sae
VF Induction vs no VF Induction: 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. VF Induction vs no VF Induction: serious adverse events. Trial comparisons, record NCT00661037-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00661037-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 | 0.25 | 0.222 | 0.28 | wilson | |
| Risk in group 2 | 0.138 | 0.12 | 0.158 | wilson | |
| Risk difference, group 1 minus group 2 | 0.112 | 0.0776 | 0.147 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.81 | 1.51 | 2.17 | log | |
| Odds ratio, group 1 over group 2 | 2.08 | 1.67 | 2.61 | log | |
| Number needed to harm, for one more participant with a serious adverse event on VF Induction than on no VF Induction | 8.92 | 6.78 | 12.9 | 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 | VF Induction | Patients having VF induction with shock termination at implant (Implantable defibrillator: Implantable defibrillator to reduce ventricular arrhythmias via shock) | 209 | 836 | EG000 |
| Group 2 | no VF Induction | Patients not having VF induction at implant or during follow-up (Implantable defibrillator: Implantable defibrillator to reduce ventricular arrhythmias via shock) | 177 | 1,284 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 2 years
Source ClinicalTrials.gov
Trial
- Title
- SAFEty of Two Strategies of ICD Management at Implantation
- NCT number
- NCT00661037
- Phases
- Conditions
- Ventricular Fibrillation, Ventricular Flutter, Sudden Cardiac Death
- Interventions
- Implantable defibrillator, Implantable defibrillator
- Lead sponsor
- Boston Scientific Corporation
- Results first posted
- 2017-06-20
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00661037?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/NCT00661037-sae