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Gut Derived Hormones, Body Composition and Metabolism in Prader-Willi Syndrome
Contribution of a GLP-1 Agonist to Appetite Regulation, Metabolism and Body Composition in Subjects With Prader-Willi Syndrome.
Lead sponsor
Assets
Exenatide / GLP-1 / incretin class catch-all
Listed sites
1
Recruiting sites
—
Enrollment
20
actual
Study population
Healthy volunteers, Hypothalamic / syndromic obesity
Key I/E criterion
—
Primary endpoint
•Satiety hormones
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
Exclusion criteria
Endpoints (2)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Other (unclassified)
2 endpointssatiety hormones
Time frame:1 day
descriptive
appetite (visual analogue scale) insulin secretion
Time frame:1 day
descriptive
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.