Sign in
Taking people in United StatesPhase 3

Comparing two blood pressure pills for high blood pressure after childbirth

Compares nifedipine and labetalol tablets in new mothers with high blood pressure.

Key facts

Who runs it
Loma Linda University
Where
Loma Linda, United StatesSee the site
Trial code
Registry title
Safest Choice of Antihypertensive Regimen for Postpartum Hypertension
Status
Recruiting
Phase
Phase 3
People taking part
500 people, planned
Started
8 May 2023
Expected to end
Dec 2027
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • Oral Nifedipine
  • Oral Labetalol
Record updated
4 February 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for women who have high blood pressure after giving birth and need medicine to control it. It compares two blood pressure medicines.

Age
18 years or older
Sex
Women only
Disease stage
High blood pressure after delivery of the placenta that needs treatment, or long-term high blood pressure after birth that needs medicine. Treatment-level pressure means 140 or higher on top or 90 or higher on the bottom on at least 2 occasions at least 4 hours apart, or 160 or higher on top or above 110 on the bottom for more than 15 minutes.

Main reasons for not taking part

  • History of moderate persistent asthma, coronary artery disease, heart failure, AV heart block or pulmonary edema
  • Cannot take Nifedipine or Labetalol
  • Heart rate below 60 or above 110
  • Native language other than English or Spanish

The registry criteria, word for word

Show all 6 criteriaShow less

Who can take part

  • Female
  • Women who develop postpartum hypertension* after delivery of the placenta or chronic hypertensive postpartum women who require medication for blood pressure control; Postpartum hypertension requiring treatment are defined as systolic blood pressure greater than or equal to 140mmHg or diastolic blood pressure greater than or equal to 90mmHg on at least 2 occasions at least 4 hours apart, or systolic blood pressure greater than or equal to 160mmHg or diastolic blood pressure greater than 110mmHg sustained for more than 15 minutes

Who cannot take part

  • History of moderate persistent asthma, coronary artery disease, heart failure, AV heart block, pulmonary edema
  • Contraindication to either Nifedipine or Labetalol
  • HR <60 or >110
  • Native language other than English or Spanish

Where in United States

  • Loma Linda University HealthLoma Linda, United StatesContact: Ashra TugungTaking people

About the trial

What the trial wants to find out

The purpose of this investigator-initiated randomized control trial is to determine whether oral Nifedipine versus oral Labetalol is superior in controlling high blood pressures in the postpartum period.

The 2 groups in the trial

  • Oral NifedipineExisting treatment, for comparison

    Participants will receive oral nifedipine for blood pressure control. Dosage may initially start at one 10mg capsule by mouth three times per 24 hours (total of 30mg a day), however dosage may be increased by 30mg increments (i.e. 20mg capsule three times a day for a total of 60mg a day). Maximum dosage for oral Nifedipine will be 120mg per day.

  • Oral LabetalolExisting treatment, for comparison

    Participants will receive oral labetalol for blood pressure control. Dosage may initially start at one 200mg tablet by mouth two times per 12 hours (total of 400mg every a day), however dosage may be increased by 100-200mg increments at a time. Maximum dosage for oral labetalol will be 2400mg per day.

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?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Safest Choice of Antihypertensive Regimen for Postpartum Hypertension: A Randomized Control Trial (SCARPH)
Plain-language title
Comparing two blood pressure pills for high blood pressure after childbirthGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
4 February 2026