Ignite Creation Date:
2024-05-05 @ 4:59 PM
Last Modification Date:
2024-10-26 @ 9:26 AM
Study NCT ID:
NCT00362557
Status:
COMPLETED
Last Update Posted:
2019-09-23
First Post:
2006-08-09
Brief Title:
Imaging Techniques in Body Magnetic Resonance Imaging MRI
Sponsor:
Johns Hopkins University
Organization:
Johns Hopkins University
Study Overview
Official Title:
Body Magnetic Resonance MR Imaging Techniques
Status:
COMPLETED
Status Verified Date:
2019-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Any patient already receiving a scheduled MR scan of the body for any clinical indication will be eligible for this program
Detailed Description:
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 areaorgan 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 areaorgan 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
Patients would not be required to make any additional visits beyond their clinically-indicated visits The study duration would vary according to the body areaorgan 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None