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Cervix Uteri "Resistance" Measurements

NCT03948932 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2022-02-07

No results posted yet for this study

Summary

Pregnant women at term, after 37 weeks' gestation will undergo cervical ripening for labor induction via cervical ripening balloon. Transvaginal sonography will be performed before balloon insertion. During balloon insertion and after uterine balloon inflation a pressure watch will be attached to the balloon and inflation pressures of the vaginal balloon will be measured and documented.

Conditions

  • Induction of Labor Affected Fetus / Newborn

Interventions

DEVICE

Transvaginal sonography

Measurement of cervical length via transvaginal sonography prior to labor induction.

DEVICE

Pressure watch

Measurement of inflation pressure in a cervical ripening balloon is PSI units.

Sponsors & Collaborators

  • Rambam Health Care Campus

    lead OTHER

Principal Investigators

  • Roy Lauterbach, MD · Rambam healthcare campus

Eligibility

Min Age
18 Years
Max Age
44 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-01
Primary Completion
2023-12-31
Completion
2024-04-01

Countries

  • Israel

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 NCT03948932 on ClinicalTrials.gov