Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
40 participants
OBSERVATIONAL
2023-12-01
2025-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Non intervention, Observational study
Non intervention, Observational study
Eligibility Criteria
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Inclusion Criteria
2. Clinical diagnosis of Angelman Syndrome and molecular confirmation of the diagnosis.
3. The participant has an acceptable guardian capable of giving consent on behalf of the participant,
4. Willingness and ability of their guardians to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
Exclusion Criteria
2. Patients who are participating in parallel studies with investigational drugs.
3. Unwillingness or inability of their guardians to follow the procedures outlined in the protocol.
3 Months
99 Years
ALL
No
Sponsors
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Parc Taulí Hospital Universitari
OTHER
Puerta de Hierro University Hospital
OTHER
Responsible Party
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BELEN RUIZ-ANTORAN
Principal Investigator
Principal Investigators
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BELEN RUIZ ANTORAN, MD, Ph
Role: PRINCIPAL_INVESTIGATOR
Clinical Pharmacology Deparment, Hospital Universitario Puerta de Hierro Majadahonda
Locations
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Hospital Parc Tauli. Servicio de Genética molecular
Barcelona, , Spain
Servicio de Farmacología Clínica. Hospital Universitario Puerta de Hierro Majadahonda
Madrid, , Spain
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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01_FAST SPAIN
Identifier Type: -
Identifier Source: org_study_id
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