Skip to content

The Fetal EKG Study

The Fetal EKG Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02320279
Enrollment
900
Registered
2014-12-19
Start date
2013-10-31
Completion date
2023-12-31
Last updated
2021-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor

Keywords

Fetal Heart Rate, Fetal EKG, FHR tracing, fetal R-waves

Brief summary

The objective is to contribute data to ongoing research activities focused on identification of EKG waveform changes in the context of clinical conditions and maternal medication use. Additionally, to develop the capacity to measure contractions more accurately and more reliably using skin-surface electrodes.

Detailed description

Specific Aim 1: To develop a technique for the quantitative analysis of fetal heart-rate (FHR) data recorded during labor using advanced mathematical techniques, including pattern-recognition analysis. * Specific Aim 2: To develop the capacity to measure fetal cardiac data using EKG sensors applied to the maternal abdomen during labor. * Specific Aim 3: To validate prenatal non-invasive measurement of the fetal QTc interval. * Specific Aim 4: To develop and validate the capacity to measure uterine contractions using the uterine EMG signal recorded from maternal skin-surface electrodes. * Specific Aim 5: Collect clinical data related to medication usage and hypoxia.

Interventions

Use of a system that monitors fetal heart rate through use of fetal EKG read using abdominal electrodes

Sponsors

Mindchild Medical Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women who are pregnant or in labor who are having their fetus' heart rate monitored continuously and able to consent * 18 years old or older. * Gestational age of 24-42 weeks. * Any method of fetal heart rate monitoring. * Pregnant women in labor as well as women who are not in labor. * Pregnant women who are admitted to labor and delivery for scheduled c-sections.

Exclusion criteria

* Women unable to consent * Women under sedation or systemic anesthesia, and women who have diminished cognitive capacity * Women in extremis (in severe pain, etc.) * Women who are using the Mindchild device for clinical monitoring.

Design outcomes

Primary

MeasureTime frameDescription
Quantitative FHRDuring LaborQuantitative analysis of fetal heart-rate data recorded during labor using advanced mathetmatical techniques, including pattern-recognition analysis using EKG electrodes applied to the maternal abdomen.

Secondary

MeasureTime frameDescription
Uterine contractionsDuring laborUterine contractions will be identified by analyzing data from surface electrodes to identify patterns consistent with uterine muscle coordinated shortening. These data will be compared to data from either the external tocometer or the internal IUPC. Cross correlation analysis will be used to compare the two signals and validate the analysis of uterine EMG signal.

Countries

United States

Contacts

Primary ContactAdam Wolfberg, MD
adam.wolfberg@mindchild.com781-624-8000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026