Measuring uterine tone during cesarean delivery
Use of a Durometer to Measure Uterine Tone in Cesarean Delivery
This study is testing a new tool to measure the tightness of the uterus during scheduled cesarean deliveries to see if it gives more accurate results than the usual method.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | Female |
| Sponsor | University of Chicago Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Trial ID | NCT06284421 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a durometer, specifically a Shore durometer, to quantitatively measure uterine tone in patients undergoing scheduled cesarean deliveries. The research aims to validate this instrument against the commonly used qualitative scoring scale for uterine tone, which has shown good reliability in previous studies. By comparing the durometer measurements with clinical assessments, the study seeks to establish a more accurate method for assessing uterine tone during cesarean sections.
Who should consider this trial
Good fit: Ideal candidates are women aged 18-50 undergoing scheduled cesarean deliveries at the University of Chicago Family Birth Center.
Not a fit: Patients undergoing unscheduled cesarean deliveries or those outside the age range of 18-50 may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved monitoring of uterine tone, potentially reducing complications associated with cesarean deliveries.
How similar studies have performed: While some studies have explored the use of durometers for measuring uterine tone, this specific application in cesarean delivery is novel and has not yet been validated.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Non-emergent (scheduled) cesarean delivery at University of Chicago Family Birth Center * Patients ages 18-50 Exclusion Criteria: * 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
Where this trial is running
Chicago, Illinois
- University of Chicago — Chicago, Illinois, United States (Recruiting)
Study contacts
- Principal investigator: Naida Cole, MD — University of Chicago
- Study coordinator: Al McAuley
- Email: amcauley1@dacc.uchicago.edu
- Phone: (773) 834-3274
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.