UnknownNCT04768803
Ghrelin in Patients With a Rare Disease Associated With Intellectual Disability, and Hyperphagia, and/or Overweight, and/or Obesity
Studying Angelman syndrome due to a point mutation
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 Hospital, Toulouse
- Principal Investigator
- Maithé TAUBER, MDUniversity Hospital, Toulouse
- Intervention
- acylated and unacylated ghrelin dosages(biological)
- Enrollment
- 300 enrolled
- Eligibility
- 3-50 years · All sexes
- Timeline
- 2021 – 2023
Study locations (2)
- Centre N°1 : 40 Centre de Référence PRADORT Pr Tauber - Toulouse Centre N°2 : 22 Centre de Référence PRADORT Pr Poitou Bernert - Paris La Pitié Salpetrière Centre N°3 : 15 Centre de Référence DI de causes rares Dr Heron - Paris La Pitié Salpêtrière Centr, Paris, France
- Tauber, Toulouse, France
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.
Open NCT04768803 on ClinicalTrials.govOther trials for Angelman syndrome due to a point mutation
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