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Clinical Trial Summary

I-123-MIBG is used to image patients with neuroblastoma, pheochromocytoma and other neural crest tumors


Clinical Trial Description

Entry criteria--Histologically documented neuroblastoma or pheochromocytoma or strong suspicion of neuroblastoma or pheochromocytoma.

Exclusion criteria--Pregnancy Randomization--None Procedure--Patients will receive a dose of I-123-MIBG by intravenous injection. Images will obtained at 18-24 hours after administration of the drug and at 42-48 hours as needed. SSKI will be used to block thyroid uptake of free I-123-iodide ;


Study Design

Observational Model: Case-Only


Related Conditions & MeSH terms


NCT number NCT00590096
Study type Observational
Source Children's Hospital Medical Center, Cincinnati
Contact
Status Completed
Phase N/A
Start date January 1991
Completion date December 2008

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