Application of Cervical Elastography in Obstetrics
Completed
Conditions studied: Cervical Elastography
In brief
The purpose of this study is to develop cervical elastography nomograms using Samsung's novel technology "E-cervix" and determine its ability to predict preterm birth. During each sonogram in which cervical lengths are measured, 5 additional cervical indices will be collected using Samsung's E-cervix technology. Each index will then be separated based on characteristics to create a nomogram for singletons, twins, and those with interventions already in place (i.e. cerclage and/or progesterone) at the time of their E-cervix assessment.
Key facts
- Study ID
- NCT03902587
- Run by
- NYU Langone Health
- People needed
- 1000
- Starts
- 2019-03-04
- Expected to finish
- 2021-01-25
- Last updated by the study team
- 2021-02-03
Who can join
Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women who present for early screening or level II ultrasound, aged 18 to 50 years, provides written Informed consent and is willing to comply with protocol requirements, and obtained cervical length and measurements using the E-cervix software/hardware
You may not qualify if…
- >50 years old
- prior cervical surgical procedures (i.e. LEEP procedure, cold knife cone biopsy)
Where it is running
- NYU Winthrop Hospital — Mineola, New York, United States
Full record on ClinicalTrials.gov
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