Noninvasive Monitoring of Uterine Activity and Fetal Heart Rate

NCT05782296 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2025-03-27

No results posted yet for this study

Summary

A clinical study designed to validate the safety and performance of the TrueLabor™ device in monitoring labor vs. current standard of care.

Conditions

  • Fetal Heart Rate or Rhythm Abnormality Affecting Newborn During Labor
  • Uterine Contractions
  • Obstetric Complication

Interventions

DEVICE

TrueLabor

Non invasive monitoring device

Sponsors & Collaborators

  • OB-Tools Ltd.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-02-24
Primary Completion
2024-06-05
Completion
2024-06-05

Countries

  • United States
  • Israel

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 NCT05782296 on ClinicalTrials.gov