Status:

COMPLETED

Magnevist (SH L 451A) Intra-individual Dose Comparison Study in Magnetic Resonance Angiography

Lead Sponsor:

Bayer

Conditions:

Magnetic Resonance Angiography

Peripheral Vascular Diseases

Eligibility:

All Genders

20+ years

Phase:

PHASE2

Brief Summary

The objective of the study was to compare the efficacy of Magnevist (SH L 451 A) at doses of 0.1 mmol/kg and 0.2 mmol/kg in contrast-enhanced 3D-Magnetic Resonance Angiography in three regions (abdomi...

Eligibility Criteria

Inclusion

  • Patients who are scheduled to undergo contrast-enhanced 3D-Magnetic Resonance Angiography

Exclusion

  • Patients with an ankle brachial pressure index (ABPI) of 0.3 or less
  • Patients with allergy to contrast media
  • Patients with serious hepatic impairment
  • Patients with serious renal impairment

Key Trial Info

Start Date :

July 1 2004

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2004

Estimated Enrollment :

12 Patients enrolled

Trial Details

Trial ID

NCT00652418

Start Date

July 1 2004

End Date

October 1 2004

Last Update

October 14 2013

Active Locations (3)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (3 locations)

1

Hirosaki-shi, Aomori, Japan, 036-8563

2

Funai-gun, Kyoto, Japan, 629-0197

3

Hamamatsu, Shizuoka, Japan, 431-3192

Magnevist (SH L 451A) Intra-individual Dose Comparison Study in Magnetic Resonance Angiography | DecenTrialz