Hormone study aims to unlock Prader-Willi feeding mystery
NCT ID NCT02529085
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study looked at how appetite-regulating hormones change in infants with Prader-Willi syndrome during the first four years of life. Researchers collected blood samples from 215 infants to understand why they switch from poor feeding to severe overeating and obesity. The goal is to identify the underlying causes and pave the way for future treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help explain why children with Prader-Willi syndrome go from poor feeding to severe overeating, pointing toward future treatments.
- What could go wrong
- This is an observational study, not a treatment trial. It may not directly lead to therapies, and results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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215 people
The number who actually took part.
- Started
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Mar 2013
- Finished
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Jun 2017
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Up to 18 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria (PWS infants cohort) * Genetic diagnosis of Prader-Willi syndrome Exclusion Criteria (PWS infants cohort) * none Inclusion Criteria (control group) * children hospitalized for a planned surgery for malformation, orthopaedic or visceral surgery Exclusion Criteria (control group) * children with endocrine disorder
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Department of Endocrinology / University Children's Hospital
Essen, Germany
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Department of Pediatrics / Division of Endocrinology
Toulouse, Haute-Garonne, 31000, France
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Department of Pediatrics / Division of Endocrinology / Erasmus University Medical Center / Sophia Children's Hospital Rotterdam
Rotterdam, 3015 GJ, Netherlands
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Karolinska University Hospital
Stockholm, Sweden
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Metabolic & Molecular Imaging Group / MRC Clinical Sciences Centre / Imperial College London / Hammersmith Hospital
London, W12 0NN, United Kingdom
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Unité d'Endocrinologie Pédiatrique / Université Catholique de Louvain
Brussels, 1200, Belgium
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Would families trade daily growth hormone shots for weekly ones?
- Can a pill tame the relentless hunger of Prader-Willi syndrome?
- Can early parent coaching help infants with rare genetic disorders thrive?
- Newborn screening study aims to catch rare diseases at birth
- Brain and eye clues to emotion recognition in autism and psychosis
- New group therapy aims to tame meltdowns in Prader-Willi teens