Imaging Techniques in Body MRI

This study is currently recruiting participants. (see Contacts and Locations)
Verified March 2012 by Johns Hopkins University
Sponsor:
Information provided by (Responsible Party):
David A. Bluemke, Johns Hopkins University
ClinicalTrials.gov Identifier:
NCT00362557
First received: August 9, 2006
Last updated: March 28, 2012
Last verified: March 2012

August 9, 2006
March 28, 2012
September 2001
December 2015   (final data collection date for primary outcome measure)
Magnetic resonance signal [ Time Frame: At time of MRI ] [ Designated as safety issue: No ]
Magnetic resonance imaging acquires signal from the human body. The signal will be measured at the time of the patient study. The amount of signal change will be measured between subjects.
Not Provided
Complete list of historical versions of study NCT00362557 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Imaging Techniques in Body MRI
Imaging Techniques in Body MRI

Any patient already receiving a scheduled MR scan of the body for any clinical indication will be eligible for this program. If patients agree to participate in this program, it would require only a slightly longer examination time. This time would vary according to the body area/organ being visualized but would not exceed 30 minutes over the length of the clinical examination. Volunteers are eligible if they are willing to undergo an MR examination.

Patients would not be required to make any additional visits beyond their clinically-indicated visits. The study duration would vary according to the body area/organ visualized but would not exceed 30 minutes over the length of the clinical examination. Volunteers would be required to keep one study appointment to include one MR imaging examination.

There will be no interruption to the standard care given to patients who participate in this trial since the clinical portion of their examination will be completed prior to the study portion of the exam.

Not Provided
Interventional
Not Provided
Allocation: Non-Randomized
Intervention Model: Factorial Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Clinically Indicated MR Imaging
Device: MRI
Magnetic resonance imaging
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
1000
December 2017
December 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male or Female clinically scheduled to undergo MR Imaging at Johns Hopkins Medical Institutions

Exclusion Criteria:

  • Contraindications to MR Imaging
Both
Not Provided
Yes
Contact: Tracy L McCracken, RN BSN CCRP 410-955-4924 tborman@jhmi.edu
United States
 
NCT00362557
01-02-07-05
Not Provided
David A. Bluemke, Johns Hopkins University
Johns Hopkins University
Not Provided
Principal Investigator: David A Bluemke, MD PhD Johns Hopkins University
Johns Hopkins University
March 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP