Építés alatt – nem éles oldal
Belépés
LeállítvaNo phase

CONNEQT Pulse Validation Study

Megadott ok: Unable to recruit intended patient population

Key facts

Where
Columbus, Egyesült ÁllamokSee the site

Where in Egyesült Államok

  • Mount Carmel EastColumbus, Egyesült ÁllamokNo longer taking part

Trial details

Who runs it
Mount Carmel Health System
Trial code
NCT06002971
Record updated
2026. március 5.
Original description
The purpose of this study is to validate the accuracy of the CONNEQT Pulse blood pressure monitoring system for the measurement of blood pressure as compared to a gold standard, auscultatory sphygmomanometer in a pregnant population.Read full original descriptionShow less

Validation of the CONNEQT Blood Pressure Monitoring System in a Pregnant Patient Population

The purpose of this study is to validate the accuracy of the CONNEQT Pulse blood pressure monitoring system for the measurement of blood pressure as compared to a gold standard, auscultatory sphygmomanometer in a pregnant population.

All Groups:; Able to provide informed consent; Pregnant patient, beyond the first trimester (greater than 12 weeks of gestation); 18 years of age, or older; Normotensive:; Systolic blood pressure <140 mmHg (18,66 kPa) and diastolic blood pressure <90 mmHg (12 kPa); Hypertensive:; Without proteinuria >300 mg in 24 h; and; With systolic blood pressure ≥140 mmHg (18,66 kPa) or diastolic blood pressure ≥ 90 mmHg (12 kPa); Pre-Eclampsia:; With proteinuria >300 mg in 24 h; and; With systolic blood pressure ≥140 mmHg (18,66 kPa) or diastolic blood pressure ≥ 90 mmHg (12,00 kPa).

ClinicalTrials.gov NCT06002971