Clinical Trials Directory

Trials / Completed

CompletedNCT00188695

Combidex USPIO - Ultra-small Superparamagnetic Iron Oxide

A Pilot Study of MR Imaging With Ultra-small Superparamagnetic Iron Oxide for Pelvic Lymph Node Target Definition

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
61 (actual)
Sponsor
University Health Network, Toronto · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test whether or not a new contrast agent called Combidex, a contrast agent formulated from ultra-small superparamagnetic iron oxide (USPIO) improves the ability of Magnetic Resonance Imaging (MRI) to see lymph nodes in the pelvis. It might also help doctors tell whether or not cancer has spread to these lymph nodes. It might allow radiotherapy to be delivered more accurately.

Conditions

Interventions

TypeNameDescription
PROCEDUREMRI contrast agent Combidex (ferumoxtran-10)Combidex as an MR-lymph node contrast agent for the detection of small lymph nodes and lymph metastases.

Timeline

Start date
2004-04-01
Primary completion
2006-06-01
Completion
2022-03-15
First posted
2005-09-16
Last updated
2022-10-07

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00188695. Inclusion in this directory is not an endorsement.