Menu
Recruiting NCT06835647

Maternal Fetal Device Performance Twins

No phase Interventional Pregnancy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Investigational Fetal Monitor, Ultrasound Imaging Device.
Who it may be relevant to
Registry conditions: Pregnancy. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Maternal Fetal Device Performance Testing During Antepartum Twin Monitoring

Overview

Maternal Fetal Monitoring devices assist the health care professional in acquiring, monitoring, and storing fetal and maternal physiologic data which support clinical decision making for pregnant women and assesses the overall fetal health status during pregnancy and delivery. This study aims to support a new maternal fetal monitoring device with clinical data by collecting simultaneous, continuous, external, distinguishable FHRs from twin pregnancies using ultrasound Doppler transducers from the new maternal fetal monitoring investigational device and a marketed ultrasound imaging device.

Detailed description

This study aims to support a new maternal fetal monitoring device with clinical data by collecting distinguishable FHRs from twin pregnancies using ultrasound Doppler transducers from the investigational device and a marketed ultrasound imaging device. This study will collect twin fetal heart rate data from the new monitor on twin gestations.

Funding for this study will be provided by GE HealthCare. This study does not include patient advisors.

Interventions

  • Device Investigational Fetal Monitor
    Investigational Fetal Monitoring Device Device is a multi-parameter maternal fetal monitor that is intended to monitor, store, display, transmit, and generate alarms for non-invasive and invasive clinical parameters of pregnant women and fetuses (singleton and twin), during the antepartum, intrapartum, and postpartum period.
  • Device Ultrasound Imaging Device
    The Ultrasound imaging device is a general-purpose diagnostic ultrasound system for use in measurement, display and analysis of the human body and fluid.

Primary outcome measures

  • Collection of Distinct Fetal Heart Rate [Time frame: 40 minutes]
  • Collection of Maternal Pulse Rate [Time frame: 40 minutes]
Secondary outcome measures (1)
  • Incidence of Safety Events [Time frame: 4 months]

Eligibility criteria

Inclusion criteria

  • Able and willing to provide written informed consent.
  • Twin pregnancy.
  • Aged 18+.
  • Greater than or equal to 30 0/7 weeks gestation.
  • Patient has none of the exclusion criteria.

Exclusion criteria

  • Non-twin pregnancy.
  • Involvement in another clinical trial currently or previously in this pregnancy that, in the investigator's opinion, would affect the conduct of this study.
  • Medical or obstetric problem that in investigator's opinion would make the patient incapable of taking part in the study.
  • Inability to understand the consent information due to medical illness, diminished intellectual capacity, or insurmountable language barrier.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

United States · 1 center
  • Element Materials Technology — Louisville

Publications

  • Ulrich CC, Dewald O. Pregnancy Ultrasound Evaluation(Archived). 2023 Feb 13. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK557572/ PMID 32491504
  • Euliano TY, Darmanjian S, Nguyen MT, Busowski JD, Euliano N, Gregg AR. Monitoring Fetal Heart Rate during Labor: A Comparison of Three Methods. J Pregnancy. 2017;2017:8529816. doi: 10.1155/2017/8529816. Epub 2017 Mar 14. PMID 28392944
  • Potchileev S, Tafti D. Sonography Fetal Assessment, Protocols, and Interpretation. 2026 Apr 15. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK576427/ PMID 35015452

Identifiers

NCT: NCT06835647 · SA-000073

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗