The Acute Cardiovascular Effects of Marathon Running Using Magnetic Resonance Imaging (MARATHON-MRI)
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
Using blood testing and cardiac magnetic resonance imaging (MRI), the investigators aim to determine if there are necrotic areas of myocardium in participants who complete a marathon. In addition, the investigators aim to describe the acute and chronic structural abnormalities that occur as a result of endurance training. The study hypothesis is that myocardial necrosis is present in runners completing a marathon competition.
| Condition |
|---|
|
Myocardial Ischemia Left Ventricular Systolic Dysfunction Elevated Cardiac Enzymes |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | The Acute Cardiovascular Effects of Marathon Running Using Magnetic Resonance Imaging |
Serum
| Enrollment: | 25 |
| Study Start Date: | September 2008 |
| Study Completion Date: | May 2010 |
| Primary Completion Date: | May 2010 (Final data collection date for primary outcome measure) |
MARATHON-MI is a prospective, observational study of twenty-five (25) participants with plans of completing the Detroit Free Press Marathon in Detroit, Michigan on October 19, 2008. All participants will undergo a rigorous pre-marathon screening process which will include: 1) blood testing, 2) complete cardiopulmonary exercise testing, 3) ECG testing, 4) Holter monitoring, 5) cardiac MRI. Blood work will be check after the marathon immediately after and one day after the event. Cardiac MRI will be repeated within 12 hours of finishing the marathon. Using the information derived from the blood work and radiological testing, we will attempt to determine if there is an association between marathon running and myocardial necrosis.
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Twenty-five (25) participants with plans of completing the Detroit Free Press Marathon in Detroit, Michigan on October 19, 2008.
Inclusion Criteria:
- Detroit Free Press Marathon participant on October 19, 2008,
- Age > 18 years old,
- Ability to provide informed consent.
Exclusion Criteria:
- Known coronary or structural heart disease
- Pregnancy,
- Extreme claustrophobia,
- Metal implants,
- Renal dysfunction.
Contacts and Locations| United States, Michigan | |
| William Beaumont Hospital | |
| Royal Oak, Michigan, United States, 48009 | |
| Principal Investigator: | Justin E Trivax, MD | Physician |
More Information
No publications provided
| Responsible Party: | Lihua QU, Coordinator, William Beaumont Hospitals |
| ClinicalTrials.gov Identifier: | NCT00752752 History of Changes |
| Other Study ID Numbers: | HIC2008-083 |
| Study First Received: | September 12, 2008 |
| Last Updated: | April 2, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by William Beaumont Hospitals:
|
Marathon Running Cardiac Ischemia Magnetic Resonance Imaging |
Additional relevant MeSH terms:
|
Myocardial Ischemia Coronary Artery Disease Ischemia Ventricular Dysfunction, Left Heart Diseases Cardiovascular Diseases |
Vascular Diseases Coronary Disease Arteriosclerosis Arterial Occlusive Diseases Pathologic Processes Ventricular Dysfunction |
ClinicalTrials.gov processed this record on May 16, 2013