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Durometer for Measuring Uterine Tone

NCT06284421 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2025-05-06

No results posted yet for this study

Summary

This study will evaluate the use of a durometer to measure uterine tone in parturients undergoing cesarean delivery.

Conditions

  • Uterine Tone Disorders
  • Cesarean Section Complications

Interventions

DEVICE

Shore durometer

The durometer will be held on the exterior of the lower uterine segment and fundus to measure the hardness reading at each location.

Sponsors & Collaborators

  • University of Chicago

    lead OTHER

Principal Investigators

  • Naida Cole, MD · University of Chicago

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2024-02-08
Primary Completion
2026-03-30
Completion
2026-08-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT06284421 on ClinicalTrials.gov