Uterine Tone DisordersPregnancyDevice
What this study is
This study will evaluate the use of a durometer to measure uterine tone in parturients undergoing cesarean delivery.
What's being tested
- Shore durometer
Intervention · 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
- Official title
- Use of a Durometer to Measure Uterine Tone in Cesarean Delivery
- Sponsor
- University of Chicago
- Conditions
- Uterine Tone Disorders · Cesarean Section Complications
- Enrolling
- 20 people
- Starts
- 2024-02-08
- Est. completion
- 2026-08-30
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years – 50 YearsSex FEMALEHealthy volunteers AcceptedYou may qualify if
- Non-emergent (scheduled) cesarean delivery at University of Chicago Family Birth Center
- Patients ages 18-50
You can't join if
- Patients undergoing unscheduled (intrapartum) cesarean delivery
- Ages <18 or >50 years old
- Intrapartum cesarean hysterectomy
- Inability to provide independent, informed consent due to impairment or intellectual disability
- Non-English speaking patients
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
Loading treatment details…
1
Study locations (1)
1 openUniversity of Chicago
Chicago, Illinois, United States
- Naida M Cole, MD · Contact773-702-6700nmcole@bsd.uchicago.edu
- Somayeh Mohammadi · Contact17738343274mohammadis@bsd.uchicago.edu
Recruiting
Study team
Sponsor
University of Chicago
Study ID IRB23-1068
Principal investigator
Naida Cole, MD
University of Chicago
Have questions? The contacts above can answer them before you apply.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.