RECRUITING

Perioperative Warming Measures in Cesarean Delivery

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

The purpose of this study is to evaluate the best method for keeping patients warm during cesarean deliveries and the effect of temperature change on the patient and baby

Official Title

Randomized Control Trial Assessing Effectiveness of Perioperative Warming Measures in Parturients Undergoing Cesarean Delivery

Quick Facts

Study Start:2021-08-23
Study Completion:2023-08-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05015582

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
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * scheduled for elective cesarean section under neuraxial anesthesia
  2. * singleton pregnancy
  1. * gestational age of less than 37 week
  2. * emergency cesarean

Contacts and Locations

Study Contact

Stacy Norrell, MD
CONTACT
(713) 500-6200
Stacy.Norrell@uth.tmc.edu

Principal Investigator

Stacy Norrell, MD
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Stacy Norrell, MD, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

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 Date2021-08-23
Study Completion Date2023-08-01

Study Record Updates

Study Start Date2021-08-23
Study Completion Date2023-08-01

Terms related to this study

Additional Relevant MeSH Terms

  • Hypothermia; Anesthesia
  • Hypothermia, Newborn
  • Hypothermia, Sequela