Electrode-Based Sensor for Non-Invasive Fetal Heart Rate Monitoring With Improved Reliability
Completed
Conditions studied: Laboring Women With Ultrasound and FSE Monitoring
In brief
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.
Key facts
- Study ID
- NCT02024165
- Run by
- OBMedical Company
- People needed
- 71
- Starts
- 2013-11-01
- Expected to finish
- 2014-04-01
- Last updated by the study team
- 2015-05-12
Who can join
Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Parturients presenting to Labor \& Delivery for labor at term (>36 weeks completed gestation)
- Single viable fetus in cephalic presentation
- With FSE or IUPC for obstetric indications
You may not qualify if…
- Multi fetal gestation
- Contraindication to FSE or IUPC placement
- Insufficient abdominal space for all required sensors
Where it is running
- Winnie Palmer Hospital for Women and Babies — Orlando, Florida, United States
Full record on ClinicalTrials.gov
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