Condition: Pre-Eclampsia; Complicating Pregnancy · Gestational Hypertension · Sponsor: Ochsner Health System
The goal of this clinical trial is to learn if patient education and regular text reminders are a feasible intervention to engage patients and reduce post partum hypertension. The main questions it aims to answer are: Is a structured postpartum remote blood pressure monitoring intervention with education and individualized medication initiation/adjustment follow-up by televisit feasible? Does a structured program reduce the occurrence of postpartum hypertension, ED visits, hospital readmissions, and adverse outcomes? Participants will: View an educational video on HDP post-delivery Receive 1-2 times daily text messages for 6 weeks postpartum Have their blood pressure medications adjusted to lower targets post partum
This description comes directly from the study's public registry record.
Salima Qamruddin, MD · +1 (504) 842-4135 · salima.qamruddin@ochsner.org
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| Ochsner Baptist | New Orleans, Louisiana, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06920563