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Ultrasound Assessment of DILAPAN-S

NCT04529837 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 44

Last updated 2023-08-09

No results posted yet for this study

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.

Conditions

  • Cervical Dilation
  • Induction of Labor
  • Ultrasound Evaluation

Interventions

OTHER

Gauze

placement of gauze

OTHER

No gauze

no gauze

Sponsors & Collaborators

  • Eastern Virginia Medical School

    lead OTHER

Principal Investigators

  • Elizabeth Seagraves, DO · Eastern Virginia Medical School MFM Fellowship

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-01
Primary Completion
2021-06-30
Completion
2021-06-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04529837 on ClinicalTrials.gov