Ignite Creation Date:
2024-05-05 @ 5:30 PM
Last Modification Date:
2024-10-26 @ 9:33 AM
Study NCT ID:
NCT00478868
Status:
COMPLETED
Last Update Posted:
2011-06-28
First Post:
2007-05-24
Brief Title:
Modic Changes and Associated Features in Southern European Chronic Low Back Pain Patients
Sponsor:
Kovacs Foundation
Organization:
Kovacs Foundation
Study Overview
Official Title:
Modic Changes and Associated Features in Southern European Chronic Low Back Pain Patients
Status:
COMPLETED
Status Verified Date:
2011-06
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:
MODIC
Brief Summary:
To assess a The prevalence of Modic changes and other findings on lumbar magnetic resonance imaging MRI among Spanish adult chronic LBP patients b Patient characteristics and radiological findings associated with Modic changes
Detailed Description:
Ten radiologists from six hospitals across six cities in Spain consecutively recruited 487 adult patients 263 women and 224 men in whom lumbar MRI had been prescribed for low back pain lasting 3 months Patients characteristics and imaging findings were assessed through previously validated instruments A multivariate logistic regression model was developed to assess the features associated with Modic changes
Outcome measures were Gender age body mass index BMI life time smoking exposure degree of physical activity and image features disk degeneration type and extension of Modic changes disk contour annular tears spinal stenosis and spondylolisthesis
Outcome measures were Gender age body mass index BMI life time smoking exposure degree of physical activity and image features disk degeneration type and extension of Modic changes disk contour annular tears spinal stenosis and spondylolisthesis
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