New blood pressure gadget put to the test in pregnancy
NCT ID NCT06002971
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study aimed to see if the CONNEQT Pulse blood pressure monitor gives accurate readings in pregnant women, including those with high blood pressure or pre-eclampsia. Researchers compared it to a standard blood pressure cuff in 41 pregnant volunteers. The study was stopped early, so the results are limited.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CONNEQT Pulse blood pressure monitoring system
- What this could lead to
- If successful, this could provide a reliable, easy-to-use blood pressure monitor for pregnant women, helping detect conditions like pre-eclampsia earlier.
- What could go wrong
- The study was terminated early with only 41 participants, so results may not be conclusive. The device may not be as accurate as standard methods in all pregnant patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
41 people
The number who actually took part.
- Started
-
Aug 2023
- Finished
-
Jun 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Pregnant patients 18 years or older and beyond the first trimester, as defined as 12 completed weeks of gestation.
- Ages
-
18 years and older
- Sex
-
Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
All Groups: 1. Able to provide informed consent 2. Pregnant patient, beyond the first trimester (greater than 12 weeks of gestation) 3. 18 years of age, or older Normotensive: 1\. Systolic blood pressure \<140 mmHg (18,66 kPa) and diastolic blood pressure \<90 mmHg (12 kPa) Hypertensive: 1. Without proteinuria \>300 mg in 24 h; and 2. With systolic blood pressure ≥140 mmHg (18,66 kPa) or diastolic blood pressure ≥ 90 mmHg (12 kPa) Pre-Eclampsia: 1. With proteinuria \>300 mg in 24 h; and 2. With systolic blood pressure ≥140 mmHg (18,66 kPa) or diastolic blood pressure ≥ 90 mmHg (12,00 kPa)
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Gestational hypertension are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Mount Carmel East
Columbus, Ohio, 43213, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Citrulline: a potential key to prolonging pregnancy in pre-eclampsia?
- Can Mom's workout shape Baby's heart health?
- Can exercise shield pregnant women from preeclampsia?
- Two proteins could give african clinics an early warning for dangerous pregnancy complication
- A bracelet and a blood pressure cuff: a simple plan to protect new mothers at risk
- Can a TB infection leave a mark on the placenta?