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NCT01830023 Clinical Trial

Vitality Trial - Sampling Examination Data

Cardiac Event Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01830023
Other study ID # 06-28
Secondary ID
Status Completed
Phase N/A
First received April 9, 2013
Last updated September 22, 2015
Start date May 2009
Est. completion date December 2013

Study information
Verified date September 2015
Source RWTH Aachen University
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Observational

Clinical Trial Summary

This study´s aim is to collect data of vitality diagnosis. A cardiac ultrasound examination will be done and the data will be compared to the other examinations.

Recruitment information / eligibility
Status Completed
Enrollment 2019
Est. completion date December 2013
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- MRI exmination outcome: positive Late Enhancement, proof of infarction scars by contrast agent.

Exclusion Criteria:

- no exclusion criteria as patients are asked to participate after evaluating the MRI examination outcome

Study Design

Observational Model: Family-Based, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Device:
• cardiac ultrasound examination
cardiac ultrasound examination to examine the vitality

Locations
Country Name City State
Germany Department of Cardiology, university hospital Aacehn North Rhine Westfalia

Sponsors (1)
Lead Sponsor Collaborator
RWTH Aachen University

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary vitality data 1 day (at time of examination) No
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