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Self-Obtained Ultrasound Scans for Measurement of Cervical Dilation and Effacement in Labor

NCT05038891 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2024-04-11

No results posted yet for this study

Summary

This is a pilot study to test the accuracy and comfort of self-directed ultrasound imaging of cervical dilation and effacement in pregnant women undergoing induction of labor. The study will assess correlation of cervical measurements between self-directed imaging and experienced provider digital cervical examinations.

Conditions

  • Cervical Dilation

Interventions

DIAGNOSTIC_TEST

Digital Cervical Exam

Standard Digital Cervical Exam by an experienced OB provider

DIAGNOSTIC_TEST

Transperineal Ultrasound

Self-administered transperineal ultrasound after instruction by a health care professional

DIAGNOSTIC_TEST

Transvaginal Ultrasound

Self-administered transvaginal ultrasound after instruction by a health care professional

Sponsors & Collaborators

Principal Investigators

  • Regan N Theiler, M.D. · Mayo Clinic

  • Megan Miller, M.D. · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-13
Primary Completion
2022-09-01
Completion
2022-12-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT05038891 on ClinicalTrials.gov