- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02179801
Screening Cardiovascular Patients for Aortic aNeurysms (SCAN) (SCAN)
Study Overview
Status
Conditions
Detailed Description
A recently published meta-analysis showed a higher prevalence of aortic aneurysm (AAA) in men requiring treatment of coronary heart disaese compared to standard population. In women, however, the prevalence was not increased. Thus, the SCAN project addresses male patients who underwent coronary artery intervention in order to screen them for the presence of an AAA using duplex sonography.
The SCAN project involves the following elements:
- Informing the patient with cardiovascular risk factors about the clinical picture of AAA
- An ultrasound scan of the abdominal aorta in patients with an increased risk for AAA
- Acquisition of patient data followed by a correlation analysis for the parameters presence of AAA and cardiovascular diseases
The cohort study is part of the SCAN project which is also conducted in an similar way by Catharina Ziekenhuis Eindhoven ClinicalTrials.gov Identifier:NCT01643317.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
Bayern
-
Munich, Bayern, Germany, 81675
- Recruiting
- Klinikum rechts der Isar, Klinik und Poliklinik für Vaskuläre und Endovaskuläre Chirurgie
-
Contact:
- Hans-Henning Eckstein, Univ.-Prof.Dr.med.
- Phone Number: 2167 0049894140
- Email: gefaesschirurgie@lrz.tum.de
-
Contact:
- Benedikt Reutersberg, Dr. med.
- Phone Number: 2166 0049894140
- Email: gefaesschirurgie@lrz.tum.de
-
Principal Investigator:
- Hans-Henning Eckstein, Prof.Dr.med.
-
Sub-Investigator:
- Benedikt Reutersberg
-
München, Bayern, Germany, 81675
- Recruiting
- I. Medizinischen Klinik und Poliklinik, Klinikum rechts der Isar der Technischen Universität München
-
Contact:
- Karl-Ludwig Laugwitz, Univ.-Prof.Dr.med.
- Phone Number: 2350 +49 (0) 89 4140
- Email: sekretariat-laugwitz@tum.de
-
Principal Investigator:
- Karl-Ludwig Laugwitz, Univ.-Prof.Dr.med.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- men with coronary artery intervention (PTCA/stenting)
- at least 1 risk factor for AAA (hypertension, hyperlipidaemia, hyperuricemia, nicotine abuse,positive family history)
Exclusion Criteria:
- life expectancy less than 1 year
- inability to follow the instructions of the investigator (dementia, lack of time, insufficient understanding of the language)
- insufficient compliance
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of AAA
Time Frame: 1 year
|
Ultrasound screen for the presence of an AAA
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of AAA in the cohort requiring treatment
Time Frame: 1 year
|
Measuring the AAA diameter
|
1 year
|
|
Correlation of risk factors for AAA with risk factors for coronary artery disease
Time Frame: 1 year
|
Therefore the cardiovascular risk factors ( diabetes, hypertension, hyperlipidaemia, hyperuricemia, nicotine abuse, positive family history, obesity) will be requested.
|
1 year
|
|
Distribution of risk factors
Time Frame: 1 year
|
Distribution of cardiovascular risk factors (diabetes, hypertension, hyperlipidaemia, hyperuricemia, nicotine abuse, positive family history, obesity) between patients with an without an AAA
|
1 year
|
|
Correlation of the number of treated vessels and AAA
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hans-Henning Eckstein, Univ.-Prof.Dr.med., Department for Vascular and Endovascular Surgery, Klinikum rechts der Isar der Technische Universität München
- Principal Investigator: Karl-Ludwig Laugwitz, Univ.-Prof.Dr.med., I. Medizinischen Klinik und Poliklinik, Klinikum rechts der Isar der Technischen Universität München
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GES_SCAN
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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-
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-
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