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Efficacy of taurine add-on therapy in Angelman syndrome

Efficacy of taurine add-on therapy in Angelman syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082614
Enrollment
Unknown
Registered
2024-04-01
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Angelman syndrome

Interventions

AS-intervention group:Taurine supplementation
Control group:Placebo

Sponsors

Hospital of Fudan University at Xiamen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 18 Years

Inclusion criteria

Inclusion criteria: ? Age 2-18 years old, male and female; ? Meeting the diagnostic criteria of AS: children with clinically and genetically confirmed AS (including four genotypes) ? Did not take any nutritional supplement containing taurine within 3 months; ? Legal guardians fully understand and sign the informed consent.

Exclusion criteria

Exclusion criteria: ? Abnormal liver and kidney function, chronic lung and heart diseases ? Use of taurine nutritional supplements or drug users in the past 3 months; ? parents or patients refused to participate in the study; ? The investigator judged that the subjects could not comply with the study requirements.

Design outcomes

Primary

MeasureTime frame
Severity of clinical symptoms in AS;sleep disorder;Feeding problems;Incidence of adverse reactions;

Secondary

MeasureTime frame
siezure;Observer-reported assessment of communication;Assessment of development;

Countries

China

Contacts

Public ContactDu Xiaonan

Children's Hospital of Fudan University at Xiamen

duxiaonan3209@163.com+86 138 1898 7304

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026