Durometer for Measuring Uterine Tone
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorUniversity of Chicago
About this trial
This study will evaluate the use of a durometer to measure uterine tone in parturients undergoing cesarean delivery.
Eligibility criteria
Qualifiers
Non-emergent (scheduled) cesarean delivery at University of Chicago Family Birth Center
Patients ages 18-50
Disqualifiers
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
Trial design
Treatments tested in this trial
- Shore durometer
Treatment groups
20 Participants
are divided into 1 treatment groupLocations
1University of Chicago60637, ChicagoIllinois, United States
Sponsors and collaborators
University of Chicago
Lead sponsor
Source ClinicalTrials.gov