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Ability of Metoprolol to Alter the Exercise Induced Elevation of Catecholamines

A Randomised, Double Blinded, Crossover Study of the Influence of Metoprolol on Exercise Induced Elevation of Catecholamines in Healthy Subjects.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00885651
Acronym
MEXICHO
Enrollment
30
Registered
2009-04-22
Start date
2008-09-30
Completion date
2009-12-31
Last updated
2009-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

SNP, catecholamines, metoprolole, healthy subjects, physiological stress

Brief 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.

Interventions

DRUGMetoprolole (Selo-Zok ®)

Tablets, 200 mg, once a day, 10 days

DRUGPlacebo

Sponsors

Danish Heart Foundation
CollaboratorOTHER
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frame
Changes in stress-triggered response of catecholamines.2 weeks and 3 days

Secondary

MeasureTime frame
Change in stress-triggered blood pressure response.2 weeks and 3 days
Change in stress-triggered pulse response.2 weeks and 3 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026