- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00469794
The Significance of Arrhythmias in Athletes (Athlete)
The Long Term Significance of Exercise Induced Ventricular Arrhythmias in Trained Athletes
Study Overview
Detailed Description
Athletes with complex ventricular arrhythmias are potentially at risk of sudden death. The risk is increased when the athletes are engaged in competitive activities.
Ventricular premature beats (VPB's) are a common finding in the athletic heart. In the majority of cases these arrhythmias are part of the "athlete's heart syndrome" and do not increase the risk of sudden death in the athletes with an apparently normal heart. The data available in the literature deal with ventricular arrhythmias assessed only by 24-h ambulatory electrocardiograms.
To date, there are no guidelines concerning athletes who develop ventricular arrhythmias during a stress test. It is unclear whether they should be allowed to continue with their competitive activity or they should be denied to do so. A study looking at the long term follow-up of these athletes will help us determine whether the development of ventricular arrhythmia during a stress test imposes any risk on the athletes.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Netanya, Israel
- Recruiting
- Wingate Institute
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Contact:
- Therese Fuchs, MD
- Phone Number: 972-8-977-9730
- Email: therese@fuchs.org
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Sub-Investigator:
- Rutie Plitz-Burstein, Ph.D.
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Competitive athletes less than 35 YO
- Competitive athletes with ventricular arrhythmias on baseline or recovery in a stress test
- Competitive athletes with ventricular arrhythmia during exercise
Exclusion Criteria:
- Athletes who don't meet the exclusion criteria.
Study Plan
How is the study designed?
Design Details
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Therese Fuchs, MD, Assaf-Harofeh Medical Center
Study record dates
Study Major Dates
Study Start
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
- 50/06
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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