CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 71 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02024165
NCT02024165N/ACompleted
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Electrode-Based Sensor for Non-Invasive Fetal Heart Rate Monitoring With Improved Reliability

OBMedical Company·observational·Posted Dec 31, 2013·Updated May 12, 2015

In Brief

An observational study for Laboring Women With Ultrasound and FSE Monitoring. Completed, enrolled 71 participants across 1 site.

Detailed Summary

The specific goal of the proposed research is to develop a reliable, non-invasive fetal and maternal heart rate and contraction monitor that is unaffected by obesity and requires less nursing intervention than the tocodynamometer and Doppler ultrasound.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsLaboring Women With Ultrasound and FSE Monitoring
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedDec 31, 2013
Enrollment StartNov 1, 2013
Primary CompletionApr 1, 2014
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 12.5 years ago