- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04738877
Cardiovascular Effects of Marathon Running (FEIDIPIDIS)
November 14, 2023 updated by: Evangelia Kouidi, Aristotle University Of Thessaloniki
FEIDIPIDIS Study: Cardiovascular Effects of Marathon Running
The aim of this study is the investigation of acute cardiovascular responses of marathon runners after the completion of a marathon race (42.2 km), as well as of the determinants of these changes.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
50
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
-
-
-
Thessaloníki, Greece
- Aristotle University Of Thessaloniki
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
Marathon runners aiming to paricipate in a marathon running race
Description
Inclusion Criteria:
- Marathon runner
Exclusion Criteria:
- Chronic disease, Drugs
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Baseline left ventricular (LV) systolic function
Time Frame: Evaluation of athletes within 3 weeks before the marathon running race.
|
Evaluation of LV ejection fraction
|
Evaluation of athletes within 3 weeks before the marathon running race.
|
Baseline LV diastolic function
Time Frame: Evaluation of athletes within 3 weeks before the marathon running race.
|
Evaluation of LV filling pressures
|
Evaluation of athletes within 3 weeks before the marathon running race.
|
Baseline basal right ventricular (RV) function
Time Frame: Evaluation of athletes within 3 weeks before the marathon running race.
|
Evaluation of tricuspid annular plane systolic excursion (TAPSE)
|
Evaluation of athletes within 3 weeks before the marathon running race.
|
Baseline global RV function
Time Frame: Evaluation of athletes within 3 weeks before the marathon running race.
|
Evaluation of RV fractional are change (RVFAC)
|
Evaluation of athletes within 3 weeks before the marathon running race.
|
Post-exercise LV systolic function
Time Frame: Evaluation of athletes immediately after the completion of the marathon running race.
|
Evaluation of LV ejection fraction
|
Evaluation of athletes immediately after the completion of the marathon running race.
|
Post-exercise LV diastolic function
Time Frame: Evaluation of athletes immediately after the completion of the marathon running race.
|
Evaluation of LV filling pressures
|
Evaluation of athletes immediately after the completion of the marathon running race.
|
Post-exercise basal RV function
Time Frame: Evaluation of athletes immediately after the completion of the marathon running race.
|
Evaluation of TAPSE
|
Evaluation of athletes immediately after the completion of the marathon running race.
|
Post-exercise global RV function
Time Frame: Evaluation of athletes immediately after the completion of the marathon running race.
|
Evaluation of RVFAC
|
Evaluation of athletes immediately after the completion of the marathon running race.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 (Actual)
February 2, 2021
Primary Completion (Actual)
August 30, 2021
Study Completion (Actual)
August 30, 2021
Study Registration Dates
First Submitted
January 27, 2021
First Submitted That Met QC Criteria
January 31, 2021
First Posted (Actual)
February 4, 2021
Study Record Updates
Last Update Posted (Actual)
November 15, 2023
Last Update Submitted That Met QC Criteria
November 14, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- EC-3/2020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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