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Targeting the beta-2 adrenergic pathway to improve skeletal muscle glucose uptake in healthy humans

Targeting the beta-2 adrenergic pathway to improve skeletal muscle glucose uptake in healthy humans - Human Beta-2 Adrenergic Stimulation and Muscle Glucose Uptake

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON50072
Enrollment
23
Registered
2019-01-09
Start date
2019-06-24
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

diabetes type 2 diabetes

Interventions

For this study, subjects will consume clenbuterol (20 microgram/capsule) or placebo tablets twice daily (40 microgram/day) for a total period of 4 weeks (2x 2 weeks).

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Caucasian; 2. Male sex; 3. Age: 18-30 years 4. BMI: 20-25 kg/m2; 5. Normal physical activity levels;

Exclusion criteria

Exclusion criteria: 1. Not meeting all inclusion criteria 2. Cardiovascular disease (determined by means of questionnaires, heart rate/blood pressure measurements and an ECG); 3. Respiratory diseases (including asthma, bronchitis and COPD); 4. Unstable body weight (weight gain or loss > 5 kg in the last three months); 5. Intention to lose or gain body weight (e.g. with caloric restriction or physical activity) 6. Excessive alcohol and/or drug abuse; 7. Hypokalaemia; 8. Anaemia; 9. Epilepsy; 10. Smoking; 11. Renal and/or liver insufficiency; 12. Participation in another biomedical study within 1 month before the first study visit, possibly interfering with the study results; 13. Medication use known to hamper subject*s safety during the study procedures; * 14. Subjects who do not want to be informed about unexpected medical findings; * 15. Subjects who do not want that their treating physician to be informed; 16. Inability to participate and/or complete the required measurements; 17. Participation in organised or structured physical exercise; 18. Any condition, disease or abnormal laboratory test result that, in the opinion of the Investigator, would interfere with the study outcome, affect trial participation or put the subject at undue risk; 19. Hyperthyroidism

Design outcomes

Primary

MeasureTime frame
Primary outcome parameter: - Insulin-stimulated peripheral glucose disposal (Rd) during the high-insulin infusion of the two-step hyperinsulinemic-euglycemic clamp

Secondary

MeasureTime frame
Secondary study parameters: - Skeletal muscle GLUT4 translocation Explorative objectives: - Body weight/composition - Plasma substrates - Heart rate and blood pressure - Insulin-mediated suppression of hepatic glucose production - (Sleeping) energy expenditure and substrate oxidation - Skeletal muscle glycogen and lipid content - Gene and protein expression in skeletal muscle - Femoral artery flow mediated dilation (FMD)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)