Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06533228
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-25
Brief Title:
Helmsley 30 Abbreviated MRE
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison of Conventional Clinical and Abbreviated MR Enterography Protocols in Children and Adults With Crohns Disease
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of our study is to compare an abbreviated magnetic resonance imaging MRI of the bowel or magnetic resonance enterography MRE protocol to a conventional standard of care MRE in children and adults with Crohns Disease
Detailed Description:
This multi-center study will evaluate the effectiveness of an abbreviated magnetic resonance imaging MRI of the bowel or magnetic resonance enterography MRE to document the presence and severity of small bowel inflammation the presence and features of stricturing and penetrating disease in children and adults with Crohns Disease
The abbreviated MRI of the bowel or MRE will not involve IV contrast or an injection of glucagon and water will replace the oral contrast used in standard of care MREs Scan time will be greatly reduced with the abbreviated MRE approximately 15 minutes compared to a standard of care MRE approximately 60 minutes
The abbreviated MRI of the bowel or MRE will not involve IV contrast or an injection of glucagon and water will replace the oral contrast used in standard of care MREs Scan time will be greatly reduced with the abbreviated MRE approximately 15 minutes compared to a standard of care MRE approximately 60 minutes
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