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Clinical Trials/NCT02179801
NCT02179801
Unknown
Not Applicable

Screening Cardiovascular Patients for Aortic aNeurysms (SCAN)

Technical University of Munich2 sites in 1 country1,000 target enrollmentMarch 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Abdominal Aortic Aneurysm
Sponsor
Technical University of Munich
Enrollment
1000
Locations
2
Primary Endpoint
Prevalence of AAA
Last Updated
9 years ago

Overview

Brief Summary

The aim of the cohort study SCAN (Screening Cardiovascular patients for Aortic aNeurysms) is to establish a screening programm for patients with a high risk for an AAA. Aortic aneurysms in these patients should be identified at an early stage and thereby AAA-associated mortality be decreased.

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: 1. Informing the patient with cardiovascular risk factors about the clinical picture of AAA 2. An ultrasound scan of the abdominal aorta in patients with an increased risk for AAA 3. 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.

Registry
clinicaltrials.gov
Start Date
March 2014
End Date
April 2018
Last Updated
9 years ago
Study Type
Observational
Sex
Male

Investigators

Sponsor
Technical University of Munich
Responsible Party
Principal Investigator
Principal Investigator

Univ.-Prof. Dr. med. Hans-Henning Eckstein

Univ.-Prof. Dr. med. Hans-Henning Eckstein

Technical University of Munich

Eligibility Criteria

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

Outcomes

Primary Outcomes

Prevalence of AAA

Time Frame: 1 year

Ultrasound screen for the presence of an AAA

Secondary Outcomes

  • Correlation of the number of treated vessels and AAA(1 year)
  • Correlation of risk factors for AAA with risk factors for coronary artery disease(1 year)
  • Prevalence of AAA in the cohort requiring treatment(1 year)
  • Distribution of risk factors(1 year)

Study Sites (2)

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