Status:

TERMINATED

3T MR Angiography of the Hepatic Vasculature

Lead Sponsor:

University of Colorado, Denver

Conditions:

Liver Blood Supply

Eligibility:

All Genders

18-70 years

Phase:

NA

Brief Summary

This study plans to learn more about the two Magnetic Resonance Angiography (MRA) techniques.

Detailed Description

This study will use two Magnetic Resonance Angiography (MRA) techniques that will look at participants liver veins and arteries without giving a coloring matter (contrast) before taking the images. In...

Eligibility Criteria

Inclusion

  • Subjects that fulfill the criteria for living liver donation and are evaluated for the procedure with CT and MR.

Exclusion

  • Unable to give informed consent
  • Unable to comply with breathing or other imaging related instructions resulting in inability to obtain diagnostic quality MRI studies
  • Not suitable to undergo MRI with a gadolinium-based contrast agent because of:
  • Claustrophobia, unless patient agrees to sedation measures per institutional standard practice during MR imaging
  • Presence of metallic objects or implanted medical devices in body per institutional safety standards
  • Weight greater than that allowable by the MR table
  • Renal failure, as determined by estimated glomerular filtration rate (eGFR) \< 30 mL/min/1.73 m2 by the Modification of Diet in Renal Disease (MDRD) model based on a serum creatinine level obtained within 28 days prior to enrollment
  • Known allergy-like reaction to contrast media (gadolinium) or moderate or severe allergic reactions to one or more allergens as defined by the American College of Radiology (ACR), and unwillingness to undergo pre-treatment as defined by the institution's policy and/or ACR guidance
  • Pregnancy (if a female is of childbearing potential --defined as a premenopausal female capable of becoming pregnant --a pregnancy test should be done)

Key Trial Info

Start Date :

July 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2017

Estimated Enrollment :

13 Patients enrolled

Trial Details

Trial ID

NCT02299934

Start Date

July 1 2014

End Date

December 1 2017

Last Update

May 7 2019

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