RecruitingNot applicableNCT06720571
Effects of Transcutaneous Vagus Nerve Stimulation on Emotion Regulation and Executive Functioning in Prader-Willi Syndrome
Studying Prader-Willi syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Bordeaux
- Principal Investigator
- Virginie Postal, PhD, LMFTUniversity of Bordeaux
- Intervention
- Auricular vagal neuromodulation therapy (aVNT)(device)
- Enrollment
- 24 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2026
Study locations (4)
- Reference Center of Prader-Willi Syndrome (PRADORT), Bordeaux, France
- Reference Center of Prader-Willi Syndrome (CRMR PRADORT), Hendaye, France
- Reference Center of Prader-Willi Syndrome (PRADORT), Paris, France
- Reference Center of Prader-Willi Syndrome (PRADORT), Toulouse, France
Collaborators
John Bost Foundation · University Hospital, Bordeaux · Hendaye hospital · Groupe Hospitalier Pitie-Salpetriere · University Hospital, Toulouse · Prader-Willi Syndrome Association
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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