Can a 'Love Hormone' spray tame Prader-Willi symptoms?
NCT ID NCT02804373
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether oxytocin nasal spray, sometimes called the 'love hormone,' can improve behavior and eating problems in adults with Prader-Willi syndrome. Fifty participants received either oxytocin or a placebo daily or every three days for 28 days. Researchers measured changes in behavior, eating habits, and brain activity using scans.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- oxytocin nasal spray
- What this could lead to
- If it works, this could offer a new way to ease behavioral and eating problems in Prader-Willi syndrome, improving social function and quality of life.
- What could go wrong
- This is a small, completed Phase 2/3 trial. Results may not be strong enough to confirm benefit, and oxytocin may not work for everyone or could have side effects like nasal irritation.
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
-
Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
50 people
The number who actually took part.
- Started
-
Jun 2014
- Finished
-
Jun 2019
- Lead sponsor
-
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
-
18 to 50 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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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: * Prader-Willi syndrome genetically confirmed * Absence of extension of the QT interval in the electrocardiogram * Absence of hypokalemia Exclusion Criteria: * Psychiatric troubles * Anomalies of the heart rhythm in significant ECG * Hepatic insufficiency * Renal insufficiency * Patients presenting a pregnancy or breast-feeding * High sensibility to OT * High sensibility to the excipients of the product * Patients having family history of genetic pathology causing an extension of the interval QT * Patients having risk factors of advanced twist
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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
-
Centre de référence Prader-Willi - Hôpital Purpan
Toulouse, 31059, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can early parent coaching help infants with rare genetic disorders thrive?
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- New group therapy aims to tame meltdowns in Prader-Willi teens