Clinical Trials Directory

Trials / Completed

CompletedNCT00126412

Meta-Iodobenzylguanidine (123I mIBG) Scintigraphy in Patients Being Evaluated for Phaeochromocytoma or Neuroblastoma

An Open-Label, Multicentre, Phase 3 Scintigraphy Study Assessing 123I-mIBG Uptake in Subjects Being Evaluated for Phaeochromocytoma or Neuroblastoma

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
251 (actual)
Sponsor
GE Healthcare · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The study is designed to study the effectiveness of 123I-mIBG as a diagnostic imaging agent in evaluating patients with known or suspected neuroblastoma or phaeochromocytoma.

Conditions

Interventions

TypeNameDescription
DRUG123I-mIBG (meta-iodobenzylguanidine)

Timeline

Start date
2005-08-02
Primary completion
2006-09-27
Completion
2006-09-27
First posted
2005-08-04
Last updated
2019-05-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00126412. Inclusion in this directory is not an endorsement.

Meta-Iodobenzylguanidine (123I mIBG) Scintigraphy in Patients Being Evaluated for Phaeochromocytoma or Neuroblastoma (NCT00126412) · Clinical Trials Directory