Ignite Creation Date:
2024-05-06 @ 1:43 AM
Last Modification Date:
2024-10-26 @ 11:08 AM
Study NCT ID:
NCT01882634
Status:
COMPLETED
Last Update Posted:
2014-11-06
First Post:
2013-06-18
Brief Title:
Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography in Primary Health Care
Sponsor:
Consorci dAtenció Primària de Salut de lEixample
Organization:
Consorci dAtenció Primària de Salut de lEixample
Study Overview
Official Title:
Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography in Primary Health Care
Status:
COMPLETED
Status Verified Date:
2014-11
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:
BarcelonAAA
Brief Summary:
To determine the prevalence of Abdominal Aortic Aneurysm AAA in the Spanish men over 60 years through a screening program in Primary Health Care using a hand-held ultrasound and to analyze the relationship between cardiovascular risk factors and cardiovascular disease in patients with AAA
Detailed Description:
Study includes a cohort of men over 60 years attented in primary health care centers of Consorci dAtenció Primària de Salut dEixample CAPSEGeneral practitioners complete an ultrasonography training in an ultrasound unit under supervision of experienced radiologists using a standard ultrasound equipment and hand-held ultrasound Trademark VScan Manufacturer General Electric USA All images and video are blindly evaluated by a radiologist in order to establish the concordance in the interpretation of images between general practitioners and radiologist Kappa index will be used to study the agreement on the presence or absence of AAA Multivariate logistic regression analysis will be used to determine the factors that influence the presence of AAA
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