Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06971991

qDSA Blood Flow Measurement in Patients Undergoing TAE of the Liver

Led by University of Wisconsin, Madison · Updated on 2026-03-30

20

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

Sponsors

U

University of Wisconsin, Madison

Lead Sponsor

S

Siemens Medical Solutions

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this research is to evaluate a new technique, quantitative digital subtraction angiography (qDSA), to measure blood flow during liver embolization procedures. Liver embolization is a way of treating liver tumors by blocking blood flow to it. The qDSA technique could help doctors ensure the blood flow to the tumor is decreased by the right amount by calculating blood flow before, during, and after the procedure. Up to 20 participants will be enrolled for 1 study visit and data collection for up to 6 months.

CONDITIONS

Official Title

qDSA Blood Flow Measurement in Patients Undergoing TAE of the Liver

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Give voluntary, written informed consent to participate in this study and willing to comply with study-related evaluation and procedure schedule
Not Eligible

You will not qualify if you...

  • Pregnancy or breastfeeding
  • Patients with an acute kidney injury or stage IV or V chronic kidney disease (creatinine greater than 2.4 or estimated glomerular filtration rate less than 30), unless anuric and on dialysis without expected return of renal function
  • Patients with an iodinated contrast allergy who cannot be adequately premedicated to receive contrast as part of the embolization procedure
  • Patients with a physical or psychological condition that would impair study participation
  • The patient is judged unsuitable for study participation by the Investigator for any other reason

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UW Hospital and Clinics

Madison, Wisconsin, United States, 53792

Actively Recruiting

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Research Team

R

Radiology Coordinators

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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