Al18F-NOTA-LM3 PET/CT in Patients With Pheochromocytoma and Paraganglioma

Recruiting N/A Interventional Study
Pheochromocytoma/Paraganglioma (PPGL)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 80
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
40 (estimated)
Sponsor
Peking Union Medical College Hospital · Other
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About This Trial

The aim of this study is to evaluate the diagnostic performance of Al18F-NOTA-LM3 PET/CT and compare it with 68Ga-DOTATATE PET/CT in patients with pheochromocytoma/paraganglioma (PPGL).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients aged 18 to 80 years. * Suspected or confirmed PPGL patients. Exclusion Criteria: * Combined with other types of tumors. * Severe liver or renal dysfunction (ALT/AST≥5 ULN, GFR\<30ml/min). * Pregnant or breast-feeding women. * Inability to perform PET/CT scans.
Contacts

Hongli Jing

18600586399

annsmile1976@sina.com

CONTACT

Yuwei Zhang

18511071577

ywzhangwork@163.com

CONTACT