Clinical Trials Directory

Trials / Completed

CompletedNCT00707876

Magnetic Resonance Angiography for Peripheral Arterial Disease (PAD)

Phase II, Open Label, Randomized, Multicenter Trial Comparing Noncontrast MRA vs. Ferumoxytol Vascular Enhanced MRI for Detection of Stenosis or Occlusion of the Aortoiliac and Superficial Femoral Arteries in PAD Subjects Scheduled for DSA

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
119 (actual)
Sponsor
AMAG Pharmaceuticals, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the difference between two magnetic resonance imaging (MRI) techniques for visualizing arteries. The study hypothesizes that one method that relies upon imaging flowing blood in the pelvic and leg arteries will not be as accurate or efficient as injecting a safe imaging agent to change the appearance of the blood on the MRI. Both methods will be compared with Digital Subtraction Angiography (DSA).

Detailed description

This was a Phase 2, open-label, randomized, multicenter study to evaluate the efficacy and safety of a single administration of intravenous (IV) ferumoxytol at 3 dose levels as a VE-MRI imaging agent to facilitate detection of arterial stenosis in subjects with PAD. Eligible subjects were already scheduled for DSA to be completed within 14 days of the MR assessments. Nineteen sites randomized subjects in the study. The sites were selected such that an equal number of subjects could be scanned on the 3 major MRI 1.5 T platforms (Siemens, General Electric, and Philips). Subjects were stratified by imaging platform and randomized to receive 1.0, 2.5, or 4.0 mg/kg IV ferumoxytol. On the same study day, subjects first underwent a noncontrast MRA, followed by administration of the randomized ferumoxytol dose and VE-MRI. Within 2 weeks subjects then underwent the previously scheduled DSA of the aortoiliac and superficial femoral arteries that served as the reference "gold standard."

Conditions

Interventions

TypeNameDescription
DRUGferumoxytol1.0 mg/kg IV ferumoxytol
DRUGferumoxytol2.5 mg/kg IV ferumoxytol
DRUGferumoxytol4.0 mg/kg IV ferumoxytol

Timeline

Start date
2008-09-01
Primary completion
2010-07-02
Completion
2020-08-15
First posted
2008-07-01
Last updated
2026-04-16
Results posted
2026-04-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00707876. Inclusion in this directory is not an endorsement.