Comparative Study Between Prader-Willi Patients Who Take Oxytocin Versus Placebo
NCT ID: NCT01038570
Last Updated: 2017-05-12
Study Results
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Basic Information
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COMPLETED
PHASE2
24 participants
INTERVENTIONAL
2009-06-30
2009-09-30
Brief Summary
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The objectives of this project are:
1. to look for an influence on the understanding of the social codes of the PWS patients,
2. to look for an influence on the behavior of stress and anxiety and on the regulation of eating habits when patients receive a nasal pulverizing of OT.
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Detailed Description
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Objectives: The objectives of this project are to investigate whether the administration by intra-nasal spray of OT plays a role on the understanding of social codes of PWS adult patients. We also analyze its effect on the level of stress, anxiety and eating behavior.
Methodology: This study is a double blind control study. We will include 24 PWS patients, aged over 18 years recruited at the Hendaye Marine Hospital (associated with the PWS reference center whose coordination is in Toulouse). The hospital routinely receives PWS adults for a 4 weeks stay which gives optimal conditions for the establishment of this study. Patients are separated into 2 groups matched one by one on the sex and IQ. One group receives the OT, the other a placebo. Forty five minutes after inhalation, all of the patients are evaluated on their social comprehension thanks to psychometric tests. Furthermore, an analysis based on observation sheets allows us to score daily stress, anxiety and eating behavior. These sheets serve for the comparison between 2 days before and 2 days after the nasal spray on the above described scoring components.
Results: Differences between the two groups will be statistically analyzed by non parametric statistical tests such as Mann-Whitney's test.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Oxytocin
Syntocinon®/- Spray
3 sprays corresponding to 24 IU in each nostril
Physiological serum
Physiological serum (Sodium chloride)
Sodium chloride 0.9 % (0.3 ml) in each nostril
Interventions
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Syntocinon®/- Spray
3 sprays corresponding to 24 IU in each nostril
Physiological serum (Sodium chloride)
Sodium chloride 0.9 % (0.3 ml) in each nostril
Eligibility Criteria
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Inclusion Criteria
* Age 18-year-old superior,
* Negative pregnancy test.
Exclusion Criteria
* Problem administration staff,
* Saving of justice,
* Abnormalities of the heart rhythm,
* Hepatic or renal insufficiency,
* Pregnancy,
* Oxytocin hypersensibility,
* Treatment causing rhythm disorders.
18 Years
ALL
No
Sponsors
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University Hospital, Toulouse
OTHER
Responsible Party
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Principal Investigators
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Maïthé TAUBER, MD
Role: PRINCIPAL_INVESTIGATOR
Centre de référence du syndrome de Prader-Willi - Equipe d'Endocrinologie
Locations
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Hôpital marin d'Hendaye
Hendaye, Pyrénées-Atlantiques, France
Countries
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References
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Tauber M, Mantoulan C, Copet P, Jauregui J, Demeer G, Diene G, Roge B, Laurier V, Ehlinger V, Arnaud C, Molinas C, Thuilleaux D. Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients. Orphanet J Rare Dis. 2011 Jun 24;6:47. doi: 10.1186/1750-1172-6-47.
Other Identifiers
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09 071 03
Identifier Type: -
Identifier Source: org_study_id
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