Ultrasound Assessment of DILAPAN-S
Completed
Conditions studied: Cervical Dilation, Induction of Labor, Ultrasound Evaluation
In brief
The goal of this observational prospective study is to assess the change in Dilapan-S rod diameters using transvaginal ultrasound over a period of 12 hours in term women undergoing induction of labor.
Key facts
- Study ID
- NCT04529837
- Run by
- Eastern Virginia Medical School
- People needed
- 44
- Starts
- 2020-10-01
- Expected to finish
- 2021-06-30
- Last updated by the study team
- 2023-08-09
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Pregnant individuals at gestational age 37 weeks or greater.
- Scheduled medical or elective induction at Sentara Norfolk General Hospital.
- Live, singleton IUP.
- Vertex presentation.
- Intact membranes.
- Bishop score of 6 or less.
You may not qualify if…
- Unwilling or unable to provide consent.
- Intrauterine fetal demise
- Contraindications to vaginal delivery.
- BMI > 45
- Vaginal bleeding
- Clinically evident genital tract infection
Where it is running
- Eastern Virginia Medical School — Norfolk, Virginia, United States
Full record on ClinicalTrials.gov
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