RECRUITING

Lower Extremity Elevation to Minimize Hemodynamic Instability During Induction of General Anesthesia

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 determine if lower extremity elevation (LEE) will reduce the incidence of postinduction hypotension, to compare the utilization of vasoactive medications after induction in patients with LEE and patients without LEE and to determine if LEE will increase measured cardiac output

Official Title

Lower Extremity Elevation to Minimize Hemodynamic Instability During Induction of General Anesthesia - a Prospective Randomized Controlled Study

Quick Facts

Study Start:2024-08-12
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06513169

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 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * American Society of Anesthesiologists (ASA)3 or lower
  2. * Patients requiring general anesthesia
  1. * Allergic reaction to drugs commonly used for general anesthesia including fentanyl, midazolam, propofol, ephedrine and phenylephrine
  2. * Pregnant women
  3. * Requiring rapid sequence induction
  4. * Prisoners
  5. * Patient refusal
  6. * Emergency Surgery

Contacts and Locations

Study Contact

Ranganathan Govindaraj, MD
CONTACT
(713) 500-6200
Ranganathan.Govindaraj@uth.tmc.edu
Erikka Washington
CONTACT
(713) 500-6202
Erikka.L.Washington@uth.tmc.edu

Principal Investigator

Ranganathan Govindaraj, 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

  • Ranganathan Govindaraj, 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 Date2024-08-12
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2024-08-12
Study Completion Date2024-12-31

Terms related to this study

Keywords Provided by Researchers

  • hypotension

Additional Relevant MeSH Terms

  • Post Induction Hypotension