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New treatment option for Pre-Eclampsia; Complicating Pregnancy
Official title Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education
ClinicalTrials.gov ID: NCT06920563
What this study is testing
- What it's testing
- 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?
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only
You may be able to join if
- Age of at least 18 years.
- Postpartum status.
- Experience new-onset hypertension during pregnancy.
- Enrollment in Connected MOM.
- Ability to provide informed consent.
You likely can't join if
- History of preeclampsia or gestational hypertension during previous pregnancy
- History of chronic hypertension
- History of coronary artery disease (myocardial infarction, coronary stent placement, coronary artery bypass grafting, spontaneous coronary artery...
- History of ischemic CVA
- History of Congestive heart failure
- Renal dysfunction
See the full eligibility criteria
- Age of at least 18 years.
- Postpartum status.
- Experience new-onset hypertension during pregnancy.
- Enrollment in Connected MOM.
- Ability to provide informed consent.
- Establish medical care within the Ochsner System to facilitate data collection.
- History of preeclampsia or gestational hypertension during previous pregnancy
- History of chronic hypertension
- History of coronary artery disease (myocardial infarction, coronary stent placement, coronary artery bypass grafting, spontaneous coronary artery dissection)
- History of ischemic CVA
- History of Congestive heart failure
- Renal dysfunction
- Liver dysfunction
- Left ventricular dysfunction
- Congenital heart disease
- Still birth at delivery
The study team makes the final eligibility decision.
Where it's taking place
- New Orleans, Louisiana, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include New Orleans, Louisiana, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.