123I-MIBG Scintigraphy in Patients Being Evaluated for Neuroendocrine Tumors

Vancouver Coastal Health2 个研究点分布在 1 个国家开始时间: 2011年6月15日最近更新: 2011年6月15日

适应症

试验速览

阶段: 3 期
发起方: Vancouver Coastal Health
试验地点: 2

研究概览研究设计入排标准研究者研究点记录与标识符相似试验

研究概览

简要总结

The study is designed to study the safety and effectiveness of 123I-MIBG as a diagnostic imaging agent in evaluating patients with known or suspected neuroendocrine tumors.

研究设计

研究类型: Interventional
主要目的: Diagnostic

入排标准

性别: All
接受健康志愿者: 否

入选标准

•Subjects must have a clinical indication for 123I-MIBG imaging to evaluate for the presence, extent, or status of neuroendocrine tumors;
•subjects must be able and willing to comply with study procedures.

排除标准

•Subjects with history of renal insufficiency (serum creatinine level > 3.0 mg/dL [265 µmol/L]) and inability to be withdrawn from medications known to interfere with 123I-MIBG uptake;
•Subjects unable to tolerate lying supine;
•Subjects pregnant or breastfeeding, unless the information to be gained outweighs the possible hazardous effects of 123I-MIBG administration. Where the assessment of the risk/benefit ration suggests the use of 123I-MIBG in nursing mothers, the breastfeeding should be discontinued for at least 48 hours post-injection.

研究者

发起方

Vancouver Coastal Health

申办方类型

Other Gov

研究点 (2)

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