Ignite Creation Date:
2025-12-24 @ 7:33 PM
Ignite Modification Date:
2025-12-29 @ 12:53 AM
Study NCT ID:
NCT03897803
Status:
UNKNOWN
Last Update Posted:
2020-10-19
First Post:
2019-03-29
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Elastography in Patients With Idiopathic Inflammatory Myopathies
Sponsor:
Benha University
Organization:
Study Overview
Official Title:
Elastography as a Follow up Imaging Tool in Patients With Idiopathic Inflammatory Myopathies
Status:
UNKNOWN
Status Verified Date:
2020-10
Last Known Status:
RECRUITING
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:
The aim of our study was to assess the performance of compression-strain US elastography in patients with idiopathic inflammatory myopathies over time and to study these findings with clinical and functional parameters as well as biochemical and electromyographic tests.
Detailed Description:
This study will be carried out on four groups:
Group (I): twenty children diagnosed to have idiopathic inflammatory myopathies(IIM)
* Group (II): twenty adults diagnosed to have IIM
* Group (III):20 healthy children matching age and sex as first control group to children with IIM .
* Group (VI):20 healthy adults matching age and sex as second control group to adults with IIM.
All patients will be evaluated at baseline at \& 4-months follow up using Semi-Quantitative strain elastography
Group (I): twenty children diagnosed to have idiopathic inflammatory myopathies(IIM)
* Group (II): twenty adults diagnosed to have IIM
* Group (III):20 healthy children matching age and sex as first control group to children with IIM .
* Group (VI):20 healthy adults matching age and sex as second control group to adults with IIM.
All patients will be evaluated at baseline at \& 4-months follow up using Semi-Quantitative strain elastography
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: