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临床试验/CTIS2024-513622-35-00
CTIS2024-513622-35-00进行中(未招募)1 期

[18F]mFBG PET-CT imaging of pheochromocytoma - 21-513

niversitair Medisch Centrum Utrecht0 个研究点目标入组 10 人开始时间: 2024年7月15日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • The patient has provided written informed consent authorization before participating in the study. - The patient is =18 years of age at the time of consent. - The patient has a diagnosis of pheochromocytoma with a known anatomical location or laboratory findings suspicious for pheochromocytoma defined as elevated serum/plasma metanefrines. - The patient should have surgery planned. - The patient should have had a CT scan not older than 8 weeks at time of the [18F]mFBG PET-CT.. - The patient has an ECOG status of Grade 0 – 2.

排除标准

  • - Patient is mentally or legally incapacitated. - Patient is pregnant or lactating. - Patient has active serious infections not controlled by antibiotics. - Patient is unable or unwilling to undergo PET-CT scanning or surgery. - Patient did receive interfering treatment between conventional CT scanning and [18F]mFBG PET-CT.

研究者

发起方
niversitair Medisch Centrum Utrecht

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mFBG PET-CT scan for the imaging of pheochromocytoma | 临床试验