Prader-Willi Syndrome
Conditions
Brief summary
The purpose of this study is to investigate the effects of a GLP-1 agonist on satiety hormones in patients with Prader-Willi Syndrome (genetic defect causing obesity).
Detailed description
Prader-Willi Syndrome (PWS) is the most frequent known genetic disorder of obesity. Hyperphagia is the main barrier to independent living in adults with PWS, and hitherto behavioural restraints and environmental modification are the only effective management measure. The emerging costs for professional care are immense. Thus, there is an urgent need for treatment which reduce appetite and food intake in this patient group. Agonists of the gut derived hormone GLP-1 which reduces food intake and causes weight loss due to slowed gastric emptying and through direct central effects. The aim of this pilot drug trial is to analyse the effect of a GLP-1 agonist on appetite regulating hormones, insulin secretion and energy expenditure before and after a meal.
Interventions
10ug Exenatide single s.c. injection
Sponsors
Study design
Eligibility
Inclusion criteria
* see below
Exclusion criteria
* Diabetes mellitus, acute infections
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| satiety hormones | 1 day |
Secondary
| Measure | Time frame |
|---|---|
| appetite (visual analogue scale) insulin secretion | 1 day |
Countries
Australia