Comparison · NCT03022526-45c3ec8a
Combined Spinal Epidural (CSE) vs Epidural: Number of Participants Currently Breastfeeding at 2 Days Postpartum (Yes/No)
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. Combined Spinal Epidural (CSE) vs Epidural: Number of Participants Currently Breastfeeding at 2 Days Postpartum (Yes/No). Trial comparisons, record NCT03022526-45c3ec8a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03022526-45c3ec8a
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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 | 0.88 | 0.7 | 0.958 | wilson | |
| Risk in group 2 | 0.643 | 0.458 | 0.793 | wilson | |
| Risk difference, group 1 minus group 2 | 0.237 | 0.00312 | 0.438 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.37 | 1 | 1.87 | log | |
| Odds ratio, group 1 over group 2 | 4.07 | 0.972 | 17.1 | log | |
| Number needed to treat, for one more participant with the outcome on Combined Spinal Epidural (CSE) than on Epidural | 4.22 | 2.29 | 320 | 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 | Combined Spinal Epidural (CSE) | intrathecal bupivacaine 2.5mg + fentanyl 15mcg followed by infusion (PCEA): bupivacaine 0.083% with fentanyl 2mcg/mL: basal 8mL/hr, demand 8mL, 2 boluses per hour allowed, total maximum hourly allowance 24mL~CSE~Bupivacaine / fentaNYL | 22 | 25 | OG000 |
| Group 2 | Epidural | epidural bupivacaine 0.083% + fentanyl 2mcg/mL (8mL) followed by fentanyl 100mcg (2mL); follwed by infusion (PCEA): bupivacaine 0.083% with fentanyl 2mcg/mL: basal 8mL/hr, demand 8mL, 2 boluses per hour allowed, total maximum hourly allowance 24mL~Epidural~Bupivacaine / fentaNYL | 18 | 28 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants Currently Breastfeeding at 2 Days Postpartum (Yes/No)
- Description
- Self-completed questionnaire, electronically completed. Results represent the percentage of each arm currently breastfeeding at this time point.
- Time frame
- 2 Days Postpartum
- Population
- This population includes all participants who completed the electronically administered breastfeeding form at the postpartum day 2 timepoint.
Source ClinicalTrials.gov
Trial
- Title
- CSE v. Epidural for Postpartum Depression
- NCT number
- NCT03022526
- Phases
- NA
- Conditions
- Depression, Postpartum, Labor Pain
- Interventions
- CSE, Epidural, Bupivacaine / fentaNYL
- Lead sponsor
- Grace Lim, MD, MS
- Results first posted
- 2020-08-10
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03022526?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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