A Safety and Efficacy Clinical Study to Evaluate the Narrowing of the Aorto-iliac Arteries While Using Gadodiamide

General Electric (GE)

Status and phase

Completed

Phase 3

Conditions

Arterial Occlusive Diseases

Aorto-iliac Stenosis

Treatments

Drug: Gadodiamide Injection

Study type

Interventional

Funder types

Industry

Identifiers

NCT00209443

SOV302

Details and patient eligibility

About

Magnetic Resonance Angiography (MRA) is an examination similar to Magnetic Resonance Imaging (MRI) which uses a magnetic field and a contrast medium when needed to visualize blood flow in the arterial vessels throughout the body.

Gadodiamide, a contrast medium, is already approved and is used to image blood vessels by directly injecting it into the vein, but this procedure has not been formally tested to image the aorto-iliac vessels using MR.

The study is designed to determine the presence or absence of a relevant stenosis (ie greater than/equal to 50%) or occlusion in aorto-iliac arteries. Intra-arterial Digital Subtraction Angiography (IADSA) will be used as the standard of truth.

Full description

GEHC has decided not to provide this detail

Enrollment

407 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Study subjects must be adults with confirmed or suspected aorto-iliac stenosis.
The subject must have been referred for Digital Subtraction Angiography.

Exclusion criteria

The subject has a known hypersensitivity to either conventional X-ray or gadolinium based MR contrast media including, but not restricted to, the investigational product.
The subject is lactating.
The subject is pregnant as defined by a serum or urine beta-HCG pregnancy test obtained within 24 hours before administration of the investigational product.
The subject received or is scheduled to receive MRI contrast medium within 24 hours prior to or less than 24 hours after administration of the investigational product.
The subject received or is scheduled to receive X-ray contrast medium within 24 hours prior to or less than 24 hours after administration of the investigational product.
The subject received an investigational product other than OMNISCAN (gadodiamide) within 30 days prior to OMNISCAN administration or will receive an investigational product within the follow-up period proposed for this study.
The subject presents any clinically active, serious, life-threatening disease with a life expectancy of less than 6 months.
The subject has a serum creatinine value of >= 3.5 mg/dL (309.4 µmol/L).
The subject has previously been included in this study.
The subject has a contra-indication for MRI according to accepted clinical guidelines.
The subject has metal implants and/or stents in the aorto-iliac region and/or hip replacement.