NCT06576544
Wearables to Define Postpartum Blood Pressure Trajectories and Facilitate Evidence-based Monitoring Guidelines
Enrolling by Invitation
Not specifiedAges 18–50ObservationalUniversity of California, San DiegoInvestigator-initiated
~300 participants
Updated 2025-11-04 on ClinicalTrials.gov
What's tested:BP Watch
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Postpartum blood pressure trends
Measured over 6 week postpartum period
Conditions
Where it's being run
1 sites across 1 statesCalifornia1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Postpartum birthing person 18 years of age or older
At least 20 weeks gestation at time of delivery
Meeting criteria for 1 of 3 risk categories for PP HTN and hypertensive morbidity
Planned postpartum care at UCSD
Exclusion
Inability to give informed consent
Institutionalization for psychiatric disorder, mental deficiency or incarcerated
Initiation of antihypertensive therapy prior to discharge from delivery hospitalization.
What this trial measures
- Postpartum blood pressure trends6 week postpartum period
Define the differences in longitudinal trends in blood pressure during the 6-week postpartum period between (a) subjects at low-risk for postpartum hypertension, (b) an intermediate-risk group, and (c) those at high-risk for postpartum hypertension.