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Buspirone Treatment of Anxiety in Williams Syndrome

Anxiety Clinical Trial

Official title:
Buspirone for the Treatment of Anxiety in Williams Syndrome

Clinical Trial Summary

The purpose of this study is to do a preliminary assessment of whether buspirone is effective, safe, and tolerable in the treatment of anxiety in children, adolescents, and adults with Williams syndrome.

Clinical Trial Description

After being informed about the study and potential risks, all patients or their legal guardians giving written informed consent will be screened for study eligibility. Patients who meet the eligibility requirements will participate in a 16-week, flexibly-dosed, open-label trial of buspirone. The dose of buspirone will be adjusted over the first 12 weeks of the study and a stable dose will be maintained for the final four weeks of the trial. Adverse effects will be reviewed at each visit and standardized measures of anxiety will be conducted at weeks 4, 8, 12, and 16. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04807517
Study type Interventional
Source Massachusetts General Hospital
Contact
Status Completed
Phase Phase 4
Start date August 1, 2021
Completion date September 11, 2023
View Details
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