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Comparison · NCT05049616-73598be6

Hctz/Lisinopril vs Extended release nifedipine: Number of Participants With Stage 2 Hypertension

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. Hctz/Lisinopril vs Extended release nifedipine: Number of Participants With Stage 2 Hypertension. Trial comparisons, record NCT05049616-73598be6. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05049616-73598be6

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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 10.2670.1420.444wilson
Risk in group 20.4290.2650.609wilson
Risk difference, group 1 minus group 2-0.162-0.3820.0796newcombe hybrid score
Risk ratio, group 1 over group 20.6220.2991.29log
Odds ratio, group 1 over group 20.4850.1611.46log
Number needed to treat, for one fewer participant with the outcome on Hctz/Lisinopril than on Extended release nifedipine6.18from 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 1Hctz/Lisinopril
Hctz/Lisinopril for postpartum management of hypertension. either a combined pill of ACE inhibitors and diuretics (Hydrochlorothiazide/Lisinopril)~ACE Inhibitors and Diuretics: Hctz/Lisinopril (brand name: Zestoretic)
830OG000
Group 2Extended release nifedipinecalcium channel blocker (Nifedipine~NIFEdipine ER: Extended release nifedipine1228OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Stage 2 Hypertension
Description
Stage 2 hypertension at day 7-10 after delivery (defined as SBP ≥ 140 and/or DBP ≥ 90 mmHg) or admission to the hospital for blood pressure control prior to day 10.~Primary outcome will be calculated as the average BP reading for day 7-10 after delivery.
Time frame
7-10 after delivery
Population
Data were not collected for 1 participants in the Hctz/Lisionpril arm. Data were not collected for 8 participants in the extended release nifedipine arm.

Source ClinicalTrials.gov

Trial

Title
Oral Combined Hydrochlorothiazide/Lisinopril Versus Oral Nifedipine for Postpartum Hypertension
NCT number
NCT05049616
Phases
PHASE4
Conditions
Hypertension in Pregnancy, Postpartum Preeclampsia
Interventions
ACE Inhibitors and Diuretics, NIFEdipine ER
Lead sponsor
The University of Texas Health Science Center, Houston
Results first posted
2023-08-14

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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