Comparison · NCT00835003-sae
38 Weeks Group vs 39 Weeks Group: 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. 38 Weeks Group vs 39 Weeks Group: serious adverse events. Trial comparisons, record NCT00835003-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00835003-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 | 0.00157 | 0.000278 | 0.00885 | wilson | |
| Risk in group 2 | 0.00313 | 0.00086 | 0.0114 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00156 | -0.00989 | 0.00606 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.502 | 0.0456 | 5.52 | log | |
| Odds ratio, group 1 over group 2 | 0.501 | 0.0453 | 5.54 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on 38 Weeks Group than on 39 Weeks Group | 640 | 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 | 38 Weeks Group | Elective caesarean section at 38 weeks and 3 days of gestation~Elective caesarean section: Procedure performed at 38 weeks and 3 days of gestation (+/- 2 days) | 1 | 636 | EG000 |
| Group 2 | 39 Weeks Group | Elective caesarean section at 39 weeks and 3 days of gestation~Elective caesarean section: Procedure performed at 39 weeks and 3 days of gestation (+/- 2 days) | 2 | 638 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 30 days
Source ClinicalTrials.gov
Trial
- Title
- Timing of Planned Caesarean Section and Morbidity of the Newborn
- NCT number
- NCT00835003
- Phases
- NA
- Conditions
- Respiratory Disorders, Intensive Care, Neonatal
- Interventions
- Elective caesarean section, Elective caesarean section
- Lead sponsor
- Aarhus University Hospital
- Results first posted
- 2014-07-03
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00835003?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/NCT00835003-sae