Durometer for Measuring Uterine Tone

Part of paid clinical trials in Chicago, Illinois.

Sponsor
University of Chicago
Study ID
NCT06284421
Status
Recruiting

Conditions

  • Cesarean Section Complications
  • Uterine Tone Disorders

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 50 Years
Healthy Volunteers
Accepted

Interventions

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

Study Details

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

Key Dates

Start date
Feb 8, 2024
Status verified
May 2025
Primary completion
Mar 30, 2026
Completion
Aug 30, 2026

Study Design

Enrollment
20 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY

Arms

  • Experimental: Durometer
    This is a single-arm trial in which a Shore durometer will be used to measure the hardness of the uterus after placental delivery during cesarean section.

Primary Outcome Measure

feasibility of a durometer [ Time Frame: within 10 minutes after placental delivery ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of ChicagoChicagoIllinois60637
Naida M Cole, MD
773-702-6700
Somayeh Mohammadi
17738343274

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