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New treatment option for Uterine Tone Disorders
Official title Durometer for Measuring Uterine Tone
ClinicalTrials.gov ID: NCT06284421
What this study is testing
- What it's testing
- This study will evaluate the use of a durometer to measure uterine tone in parturients undergoing cesarean delivery.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 50, women only. Healthy volunteers may be eligible.
You may be able to join if
- Non-emergent (scheduled) cesarean delivery at University of Chicago Family Birth Center
- Patients ages 18-50
You likely can't join if
- Patients undergoing unscheduled (intrapartum) cesarean delivery
- Ages \ 50 years old
- Intrapartum cesarean hysterectomy
- Inability to provide independent, informed consent due to impairment or intellectual disability
- Non-English speaking patients
The study team makes the final eligibility decision.
Where it's taking place
- Chicago, Illinois, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years to 50 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Chicago, Illinois, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.