Fetal MonitoringPregnancyDevice
What this study is
This is a feasibility study for a new application for capturing fetal cardiac activity. The objective of this study is to determine if it is feasible to capture a fetal ECG signal using a Holter ECG device. As comparison we will use a standard Doppler Fetal Heart Rate (FHR) device.
What's being tested
- Holter Device
Intervention · DEVICE
MyECG E3.80 Holter Recorder
Study details
- Sponsor
- University of Washington
- Conditions
- Fetal Monitoring
- Enrolling
- 50 people
- Starts
- 2017-06-02
- Est. completion
- 2026-12
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years – 55 YearsSex FEMALEHealthy volunteers Not acceptedYou may qualify if
- Singleton or twin pregnant women at 32 weeks gestation to full term after routine antepartum testing.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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1
Study locations (1)
1 openUniversity of Washington
Seattle, Washington, United States
- Martin G Frasch, MD, PhD · Contact206-543-5892mfrasch@uw.edu
- Amy Gest, MPA · Contact206-359-1961agest@uw.edu
- Martin Frasch, MD, PhD · Principal investigator
Recruiting
Study team
Sponsor
University of Washington
Study ID STUDY00001556
Principal investigator
Martin G Frasch, MD, PhD
University of Washington
Have questions? The contacts above can answer them before you apply.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.