RecruitingNCT06813742

18F-mFBG PET Imaging in the Evaluation of Pheochromocytoma

A Prospective Exploratory Study Evaluating the Diagnostic Usefulness of 18F-mFBG PET Imaging in Pheochromocytoma


Sponsor

First Affiliated Hospital of Zhejiang University

Enrollment

80 participants

Start Date

May 1, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

The aim of this study is to evaluate the diagnostic performance and tumor burden of 18F-metafluorobenzylguanidine (18F-MFBG) positron emission tomography (PET) in patients with pheochromocytoma.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria3

  • Aged 30-80 years old, primary school or above, with a regular caregiver;
  • Clinically diagnosed patients with pheochromocytoma;
  • Can provide informed consent, can understand and comply with the study requirements.

Exclusion Criteria7

  • Patients with serious primary diseases such as heart, brain, liver, kidney and hematopoietic system;
  • Uncontrolled hypertension or high-risk BP (i.e., systolic BP > 180 mmHg or diastolic BP > 110 mmHg);
  • Patients with mental disorders or primary affective disorders;
  • Unable to understand and adhere to the study protocol or provide informed consent;
  • Contraindications to PET imaging (including pregnant women, lactating women, and women of childbearing age with recent childbearing plans, etc.);
  • Allergy to imaging agents;
  • Patients who were unable to cooperate with PET scanning, such as hypoglycemia, severe pain or tremor.

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Interventions

DRUG18F-MFBG

Patients with pheochromocytoma malignancies receive 5.55 MBq/kg of 18F-MFBG intravenously followed by PET/CT or PET/MR after 60min of injection.


Locations(2)

The First Affiliated Hospital of Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

The First Affiliated Hospital Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

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NCT06813742


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