Natural History Study for Patients With Angelman Syndrome

NCT ID: NCT06229769

Last Updated: 2025-05-20

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-10-10

Study Completion Date

2028-01-31

Brief Summary

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This study is a 9-year natural history study for patients with Angelman syndrome in Belgium (a genetic neurodevelopmental disorder, affecting 500,000 individuals in the world). It includes a 3-year recruitment phase, a 5 year follow-up and a year to analyze the collected data. The investigators plan to include 30 patients with a semi-annual follow-up for 4 years.

The investigators will collect relevant retrospective and prospective data using age-standardized scales and questionnaires for functional motor assessments and global developmental assessment.

Detailed Description

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Patients are seen every six months for five years. In these visits, patient have medical review (general medical examination, neurological examination), vital signs (height, weight, respiratory rate, heart rate, blood pressure), cognitive assessment (Bayley-IV), language assessment and questionaire (Bayley-IV, ORCA), motor assessments (Bayley-IV, FMS, Developmental milestones and HINE), quality of life questionnaire (PedsQL, CGI-CASS) and general development questionnaire (Vineland-II).

Conditions

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Angelman Syndrome

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* Genetically confirmed diagnosis of AS
* 0-99 years
* Male or Female
* Participant's carer is willing to give IC/sign a "record of consultation" for participation in the study

Exclusion Criteria

* comorbidity that could potentially affect the results of the study coexists. This
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Régional de la Citadelle

OTHER

Sponsor Role collaborator

SYSNAV

INDUSTRY

Sponsor Role collaborator

Centre Hospitalier Universitaire de Liege

OTHER

Sponsor Role lead

Responsible Party

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Laurent Servais

Prof. Investigator of CRMN Liège, Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Laura Vanden Brande

Role: PRINCIPAL_INVESTIGATOR

CHR Citadelle

Locations

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CHR Citadelle Liège

Liège, Liège, Belgium

Site Status RECRUITING

Countries

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Belgium

Central Contacts

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Noor Benmhammed

Role: CONTACT

43217726 ext. +32

Tamara Dangouloff, PhD

Role: CONTACT

Facility Contacts

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Noor Benmhammed

Role: primary

43217726 ext. +32

Tamara Dangouloff, PhD

Role: backup

43215269 ext. +32

Other Identifiers

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NatHis-Angelman

Identifier Type: -

Identifier Source: org_study_id

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