Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06606834
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-11
Brief Title:
Assessment of the Uterus Using Ultrasonographic Elastography in Women with Dysmenorrhea
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Assessment of the Uterus Using Ultrasonographic Elastography in Women with Dysmenorrhea
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
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 aim of this study is to perform sonoelastographic assessment of the uterus in patients diagnosed with primary dysmenorrhea and to compare these measurements with sonoelastographic evaluations of the uteri in asymptomatic individuals This will enable for the first time the demonstration of whether the elasticity of the myometrial tissue contributes to the etiology of primary dysmenorrhea
Secondary Objectives To determine whether there is a correlation between the severity of primary dysmenorrhea and ultrasonographic markers
Secondary Objectives To determine whether there is a correlation between the severity of primary dysmenorrhea and ultrasonographic markers
Detailed Description:
None
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