CompletedNot Applicable

Ultrasound Assessment of DILAPAN-S

United States44 participantsStarted 2020-10-01

Plain-language summary

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.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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. Exclusion Criteria: * Unwilling or unable to provide consent. * Intrauterine fetal demise * Contraindications to vaginal delivery. * BMI \> 45 * Vaginal bleeding * Clinically evident genital tract infection

What they're measuring

Diameter change of Dilapan-S

Timeframe: 12 hours

Trial details

NCT IDNCT04529837

SponsorEastern Virginia Medical School

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2021-06-30

View on ClinicalTrials.gov More Cervical Dilation trials