RECRUITING

Durometer for Measuring Uterine Tone

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Use of a Durometer to Measure Uterine Tone in Cesarean Delivery

Quick Facts

Study Start:2024-02-08
Study Completion:2024-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06284421

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 50 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Non-emergent (scheduled) cesarean delivery at University of Chicago Family Birth Center
  2. * Patients ages 18-50
  1. * Patients undergoing unscheduled (intrapartum) cesarean delivery
  2. * Ages \<18 or \>50 years old
  3. * Intrapartum cesarean hysterectomy
  4. * Inability to provide independent, informed consent due to impairment or intellectual disability
  5. * Non-English speaking patients

Contacts and Locations

Study Contact

Al McAuley
CONTACT
(773) 834-3274
amcauley1@dacc.uchicago.edu

Principal Investigator

Naida Cole, MD
PRINCIPAL_INVESTIGATOR
University of Chicago

Study Locations (Sites)

University of Chicago
Chicago, Illinois, 60637
United States

Collaborators and Investigators

Sponsor: University of Chicago

  • Naida Cole, MD, PRINCIPAL_INVESTIGATOR, University of Chicago

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-08
Study Completion Date2024-12-30

Study Record Updates

Study Start Date2024-02-08
Study Completion Date2024-12-30

Terms related to this study

Additional Relevant MeSH Terms

  • Uterine Tone Disorders
  • Cesarean Section Complications