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Comparison · NCT04790279-bfa8b4f2

Amlodipine vs Nifedipine ER: Breastfeeding Duration of 6+ Weeks

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. Amlodipine vs Nifedipine ER: Breastfeeding Duration of 6+ Weeks. Trial comparisons, record NCT04790279-bfa8b4f2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04790279-bfa8b4f2

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.3330.1380.609wilson
Risk in group 20.1760.06190.41wilson
Risk difference, group 1 minus group 20.157-0.1480.456newcombe hybrid score
Risk ratio, group 1 over group 21.890.5146.94log
Odds ratio, group 1 over group 22.330.41313.2log
Number needed to treat, for one more participant with the outcome on Amlodipine than on Nifedipine ER6.38from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1AmlodipineAmlodipine Per Protocol412OG000
Group 2Nifedipine ERNifedipine ER Per Protocol317OG001

Outcome

Type
SECONDARY
Title
Breastfeeding Duration of 6+ Weeks
Description
Time frame
until 6 weeks postpartum
Population
Only includes patients who answered relevant question on breastfeeding questionnaire

Source ClinicalTrials.gov

Trial

Title
Amlodipine Versus Nifedipine ER for the Management of Postpartum Hypertension
NCT number
NCT04790279
Phases
PHASE4
Conditions
Hypertension in Pregnancy
Interventions
Amlodipine, NIFEdipine ER
Lead sponsor
Prisma Health-Upstate
Results first posted
2024-10-28

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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