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CONNEQT Pulse Validation Study

NCT06002971 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 41

Last updated 2026-03-05

No results posted yet for this study

Summary

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.

Conditions

  • Pregnancy Related
  • Pre-Eclampsia
  • Gestational Hypertension

Interventions

DEVICE

Blood pressure measurement

Serial blood pressure measurements to compare reference auscultatory sphygmomanometer to CONNEQT Pulse according to ISO 81060-2.

Sponsors & Collaborators

  • AtCor Medical, Inc.

    collaborator INDUSTRY

  • Mount Carmel Health System

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-08-21
Primary Completion
2025-06-03
Completion
2025-06-03
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06002971 on ClinicalTrials.gov