- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01617863
Hemodynamics During the Soccer Championship 2012
July 2, 2012 updated by: PD. Dr. med Michael Reppel, University Hospital Schleswig-Holstein
Central Hemodynamics, Arterial Stiffness, Heartrate and Endothelial Dysfunktion During the European Soccer Championship 2012
The purpose of this study is to determine in soccer fans whether and to which extend positive or negative emotions during the European soccer Championship affects Central Hemodynamics, Arterial Stiffness, Heartrate and Endothelial Dysfunktion.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Anticipated)
180
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Hamburg, Germany
- Universitätsklinikum Eppendorf
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Bayern
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Erlangen, Bayern, Germany, 91054
- Universitätsklinikum Erlangen
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Mecklenburg-Vorpommern
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Greifswald, Mecklenburg-Vorpommern, Germany, 17475
- Universitätsklinikum Greifswald
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Schleswig-Holstein
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Lübeck, Schleswig-Holstein, Germany, 23538
- UKSH-Lübeck
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
primary care clinic, clinical employees, students
Description
Inclusion Criteria:
Best fit:
- cardiomyopathy "severe myocardial disease leading to heart failure"
- Angina, stable for at least 7 days
- Myocardial infarction during 4 weeks before inclusion, actually stable condition
- Angina, Stable, CCS II-IV
Exclusion Criteria:
- not interested in soccer championship
- age <18y
- dementia
- atrial tachycardia
- drug/alcohol abuse
- chronic kidney disease, stage 5
- pulmonary/tricuspid valve insufficiency/stenoses
- non compliant
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Director: Michael Reppel, PD. Dr. med, UKSH- Lübeck Medizinische Klinik 2
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2012
Primary Completion (Actual)
July 1, 2012
Study Completion (Actual)
July 1, 2012
Study Registration Dates
First Submitted
June 8, 2012
First Submitted That Met QC Criteria
June 9, 2012
First Posted (Estimate)
June 12, 2012
Study Record Updates
Last Update Posted (Estimate)
July 3, 2012
Last Update Submitted That Met QC Criteria
July 2, 2012
Last Verified
June 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HL-Med2-EM-2012
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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