Actively Recruiting

Phase 1
Age: 18Years - 75Years
All Genders
NCT07456878

Use of [18F] Fluoroethyl-L-tyrosine PET/MRI for Identifying Small Functional Pituitary Adenomas

Led by Mayo Clinic · Updated on 2026-03-09

5

Participants Needed

1

Research Sites

46 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this research is to evaluate the diagnostic role and clinical efficacy of investigational FET-PET/MRI in detecting MRI-occult primary or residual/recurrent functional pituitary adenomas (PAs) and its influence on clinical and surgical decisions.

CONDITIONS

Official Title

Use of [18F] Fluoroethyl-L-tyrosine PET/MRI for Identifying Small Functional Pituitary Adenomas

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 to 75 years of age with biochemically proven Cushing's Disease, Acromegaly, or tumor hyperprolactinemia according to current Endocrinology guidelines
  • Clinical DCE-MRI protocol that is negative or equivocal for identifiable tumor
  • Patient willing to have surgery if lesion found, or already scheduled for surgery and lesion identification would be helpful
  • Able to provide informed consent and complete the imaging protocols
  • Female subjects of childbearing potential must have a negative urine pregnancy test within 48 hours prior to the 18F-FET injection
Not Eligible

You will not qualify if you...

  • Patients with contraindications to MRI or PET scans
  • Patients with known allergies to contrast agents or other imaging-related materials
  • Patients with severe medical conditions that prevent participation, such as inability to lie still for 30-60 minutes
  • Patients with successful MRI localization of the adenoma

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

Mayo Clinic

Jacksonville, Florida, United States, 32224

Actively Recruiting

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Research Team

J

Julia Santos

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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