Ability of Metoprolol to Alter the Exercise Induced Elevation of Catecholamines
Information source: Rigshospitalet, Denmark
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Heart Failure
Intervention: Metoprolole (Selo-Zok ®) (Drug); Placebo (Drug)
Phase: Phase 4
Status: Enrolling by invitation
Sponsored by: Rigshospitalet, Denmark Official(s) and/or principal investigator(s): Henrik HP Enghusen Poulsen, MD, Principal Investigator, Affiliation: Rigshospitalet, Universityhospital of Copenhagen
Summary
Heart failure is a frequent disease in Denmark, and it is associated with very high
mortality. Around 60,000 people in Denmark have heart failure, and there is about 11,000
hospitalizations every year due to this disease. From the time of diagnosis, patients
survive an average of 4-5 years.
A critical illness mechanism in heart failure is that these patients have high blood levels
of catecholamines; epinephrine and norepinephrine, which is stress hormones from the
sympathetic nervous system. Standard treatment of heart failure is with the two medical
preparations betablockers and ACE-inhibitors.
It is not known what effect betablocker-treatment have on blood concentration of epinephrine
and norepinephrine.
It is the purpose of this study, to investigate the effect of Selo-Zok ® (metoprolol) on the
blood concentration of epinephrine and norepinephrine. This is done by creating a stress
condition for the body, in this case with the bicycle test, while doing blood samples to
determine the concentration of catecholamines. This will be done by 1-week treatment of
tablet Selo-Zok ® followed by 1-week treatment of placebo (a substance with no medical
effect). Blood samples will be taken to determine small changes in inheritance material
(DNA) in the form of point mutations also called single nucleotide polymorphisms, since
these changes can affect how we respond to metoprolol treatment.
Clinical Details
Official title: A Randomised, Double Blinded, Crossover Study of the Influence of Metoprolol on Exercise Induced Elevation of Catecholamines in Healthy Subjects.
Study design: Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Changes in stress-triggered response of catecholamines.
Secondary outcome: Change in stress-triggered blood pressure response.Change in stress-triggered pulse response.
Eligibility
Minimum age: 18 Years.
Maximum age: 30 Years.
Gender(s): Male.
Criteria:
Inclusion Criteria:
- Kaukaser
- Healthy men
- 18 years < age < 30 years
- Non-smoker
- 18 < BMI < 25
- No chronic diseases
- Motor-disability that disables completement of cardio-pulmonary exercise-test.
Exclusion Criteria:
- Alcohol abuse or any other abuse
- Intake of any narcotic drugs (example: cannabinoids, narcotics, stimulants of
central nervous system, hypnotics, hallucinogenes)
- Any of following medication:
- astmamedication
- heartmedication
- antihistamines
- antipsycotics
- NSAIDs
- rifampicine
- chinidine
- glucocorticoids
- Abnormal ECG, particularly 2. or 3. degree AV-block, sinusbradycardia, sick
sinusnode-syndrome, sign of heart failure or ischemia.
- Allergy or intolerance of metoprolole
- Lactoseallergy
- 110 mmHg < Systolic blood pressure < 140 mmHg
- 60 mmHg < Diastolic blood pressure < 90 mmHg
- Bloodsucker > 11,1 mmol/L, or fasting, venous bloodsucker >= 7,0 (measured if: 7,8 <
BS < 11,1)
Locations and Contacts
Additional Information
Starting date: September 2008
Last updated: April 21, 2009
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