Angelman Natural History Study - FAST Spain

NCT ID: NCT06115109

Last Updated: 2024-04-03

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

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-12-01

Study Completion Date

2025-07-01

Brief Summary

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The goal of this study is to conduct a prospective, longitudinal study to observe the natural clinical progression and disease outcome of AS patients receiving no disease-modified intervention, with the purpose of obtaining data that will be useful for future clinical trials.

Detailed Description

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The overall goal is to increase our understanding of the long-term natural history of Angelman syndrome and to identify and validate objective and sensitive outcome measures, which could serve as endpoints for outcome measures that can be used in clinical trials.

Conditions

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Angelman Syndrome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Non intervention, Observational study

Non intervention, Observational study

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Male or female between 3 months and 99 years of age.
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

1. Patients with any comorbidity that, in the clinical judgment of the principal investigator, may affect the results of the study. Any confirmed chronic or acute condition or illness affecting any system(s) that could interfere with study results and/or compliance with study procedures is included.
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.
Minimum Eligible Age

3 Months

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Parc Taulí Hospital Universitari

OTHER

Sponsor Role collaborator

Puerta de Hierro University Hospital

OTHER

Sponsor Role lead

Responsible Party

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BELEN RUIZ-ANTORAN

Principal Investigator

Responsibility Role 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

Site Status RECRUITING

Servicio de Farmacología Clínica. Hospital Universitario Puerta de Hierro Majadahonda

Madrid, , Spain

Site Status RECRUITING

Countries

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Spain

Central Contacts

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BELEN RUIZ ANTORAN, MD, Ph

Role: CONTACT

+34911917479

Facility Contacts

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Neus Baena Diez

Role: primary

(+34) 93 6933200

Belen Ruiz Antorán, MD, Ph

Role: primary

(+34) 91 1917479

Other Identifiers

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01_FAST SPAIN

Identifier Type: -

Identifier Source: org_study_id

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