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Taking people in United StatesPhase 1

Blood Pressure Treatment Study for Mild High Blood Pressure in Pregnancy

Tests labetalol or nifedipine to lower blood pressure in pregnant people with mild hypertension.

Plain-language title generated from the registry record
Registry title: Chronic Hypertension and Pregnancy 2 (CHAP2) Pilot Project

Key facts

Where
Birmingham, United StatesSee the site
Phase
Phase 1

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 14 and 89 years old?

Source: NCT05989581, who can take part

Where in United States

  • UABBirmingham, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of Alabama at Birmingham
Trial code
NCT05989581
Record updated
11 August 2026
Original description
The CHAP2 study is designed to provide preliminary data for a larger multicenter study to assess whether treatment of stage 1 hypertension (HTN) in pregnancy improves maternal and or neonatal outcomes. The primary objective of this pilot study is to determine if anti-HTN treatment to BP<130/80mmHg in pregnant patients with stage 1 HTN is associated with a difference in birthweight percentile at delivery. Patients with stage 1 hypertension in pregnancy will be randomized to BP goals of <130/80mmHg or usual care to treatment only if BPs ≥140/90mmHg. For this pilot, the investigator will randomize a total of 74 eligible participants, 37 to active treatment to BP<130/80mmHg and 37 to usual care.Read full original descriptionShow less

Treatment of American Heart Association/American College of Cardiology Stage 1 Hypertension in Pregnancy: A Randomized Control Trial

The CHAP2 study is designed to provide preliminary data for a larger multicenter study to assess whether treatment of stage 1 hypertension (HTN) in pregnancy improves maternal and or neonatal outcomes. The primary objective of this pilot study is to determine if anti-HTN treatment to BP<130/80mmHg in pregnant patients with stage 1 HTN is associated with a difference in birthweight percentile at delivery. Patients with stage 1 hypertension in pregnancy will be randomized to BP goals of <130/80mmHg or usual care to treatment only if BPs ≥140/90mmHg. For this pilot, the investigator will randomize a total of 74 eligible participants, 37 to active treatment to BP<130/80mmHg and 37 to usual care.

Inclusion: Viable singleton gestation; No fetal anomalies; Blood pressures 130-139/80-89mmHg on two occasions at least 4 hours apart prior to 20 weeks gestation; Planning to deliver at UAB Hospital; No indication for pregnancy termination; Receiving care at the UAB prenatal clinics.

Exclusion: Fetal demise diagnosed prior to enrollment; Known major structural of chromosomal abnormalities prior to enrollment; Known diagnosis of chronic hypertension ( BP ≥ 140/90mmHg) or current antihypertensive medication use; Declines Randomization; Contraindication to first line antihypertensive (Nifedipine/ Labetalol); Comorbidities requiring BP goals < 130/80mmHg.

ClinicalTrials.gov NCT05989581