RECRUITING

CT TAVR Abdomen Study

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

A standard polyenergetic CT (computed tomography) procedure utilizes 100 ml of iodinated contrast. A recent world-wide shortage of iodine based intravenous contrast has highlighted the need to search for alternative methods or doses. Reducing iodinated IV contrast dose can mitigate IV contrast supply shortages and enable significant cost savings for the radiology practice and hospital system. In addition, decreased IV contrast dose can potentially reduce the rate of acute kidney injury, specifically in patients with decreased renal function. The purpose of the study is to determine whether low IV contrast dose CT with monoenergetic reconstruction can be use for presurgical planning of transcatheter valve replacement (TAVR) procedure.

Official Title

Dual Energy CT Decreased IV Contrast Dose Imaging for TAVR

Quick Facts

Study Start:2023-09-19
Study Completion:2026-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05758701

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 88 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * scheduled to receive TAVR abdominal CT
  1. * cannot undergo CT scan
  2. * Allergy to intravenous contrast not controlled by steroids or benadryl
  3. * GFR\<30

Contacts and Locations

Study Contact

Vikas Kundra, M.D., Ph.D
CONTACT
410-328-3477
vkundra@som.umaryland.edu
Nikita Rednam, B.S.
CONTACT
410-706-5938
nrednam@som.umaryland.edu

Study Locations (Sites)

University of Maryland Medical Center
Baltimore, Maryland, 21201
United States

Collaborators and Investigators

Sponsor: University of Maryland, Baltimore

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 Date2023-09-19
Study Completion Date2026-03-01

Study Record Updates

Study Start Date2023-09-19
Study Completion Date2026-03-01

Terms related to this study

Keywords Provided by Researchers

  • Dual energy CT

Additional Relevant MeSH Terms

  • Transcatheter Aortic Valve Replacement