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Cervical Gland Area as a Predictor of Success of Labour Induction

NCT04416022 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2020-06-04

No results posted yet for this study

Summary

Women who fulfil the inclusion criteria and who are planned for labour induction will be recruited. Bishop score, cervical length, and the presence of cervical glandular area (CGA) will be documented for every patient up to 12 hours prior to the induction process, and patient information and maternal and neonatal outcome will be documented following the delivery.

Conditions

  • Induced Vaginal Delivery

Interventions

DIAGNOSTIC_TEST

Ultrasound examination

Women that are planned for labour induction, will undergo a routine ultrasound examination prior to the initiation of the induction process.

Sponsors & Collaborators

  • Rambam Health Care Campus

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2020-06-07
Primary Completion
2022-06-07
Completion
2022-06-07

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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 NCT04416022 on ClinicalTrials.gov