het onderzoek is niet van toepassing op een klasse van aandoening(en), maar op fysiologische veranderingen gelijkend op het effect van duurtraining. not applicable
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy male volunteers, 18-50 years old, non-obese body mass (BMI 18.5-29.9 kg/m2)
Exclusion criteria
Exclusion criteria: BMI>/= 30 kg/m2, diabetes mellitus, lipid spectrum abnormalities, thyroid, kidney, or liver abnormalities, (history of) cardiovascular disease including TIA and stroke; high blood pressure or the use of antihypertensive drugs at baseline; CK-increasing drugs including statins; use of acetylsalicyl acid or non-steroidal anti-inflammatory drugs (NSAIDs) in the two week prior to the visits; neuromuscular or endocrine disorders; vasculitis; HIV infection; infectious hepatitis; personal or family history of bleeding disorders; sickle cell anaemia or other hereditary anaemia; smoking; vegetarian diet; current urse or use within 2 months prior to start of the trial of beta-guanidinopropionic acid or creatine. The participants are instructed not to perform exercise thee days prior to the basline visit and during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tolerability of GPA | — |
Secondary
| Measure | Time frame |
|---|---|
| The difference in hemodynamic parameters with GPA 100 mg vs placebo and creatine 5 g, including blood pressure, heart rate, cardiac output, and total peripheral resistance. The difference in biochemical parameters with GPA 100 mg vs placebo and creatine 5 g, including serum GPA, creatine, creatine kinase, glucose, insuline, and creatinine, and urine GPA, creatine and creatinine. The difference in ADP-dependent plateletaggregation and thrombocyt count. | — |
Countries
Netherlands