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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 21 March 2022
Main ID:  NCT00768820
Date of registration: 07/10/2008
Prospective Registration: No
Primary sponsor: The Chaim Sheba Medical Center
Public title: The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome VCFS
Scientific title: The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome (VCFS), Williams Syndrome (WS)and Fragile X Syndrome Characterization, Treatment and Examining the Connection to Developmental and Molecular Factors
Date of first enrolment: May 2001
Target sample size: 400
Recruitment status: Recruiting
URL:  https://clinicaltrials.gov/show/NCT00768820
Study type:  Interventional
Study design:  Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Diagnostic. Masking: None (Open Label).  
Phase:  Phase 4
Countries of recruitment
Israel
Contacts
Name:     Doron Gothelf, MD
Address: 
Telephone: 972-03-5302663
Email: gothelf@post.tau.ac.il
Affiliation: 
Name:     Doron Gothelf, MD
Address: 
Telephone: 972-03-5302663
Email:
Affiliation: 
Key inclusion & exclusion criteria

Inclusion Criteria:

- chromosomal deletion proven by FISH examination

Exclusion Criteria:



Age minimum: N/A
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Fragile X Syndrome
Williams Syndrome
Velocardiofacial Syndrome
Intervention(s)
Drug: methylphenidate, fluoxetin, risperidone
Primary Outcome(s)
Measure that are used: psychological measures, molecular tests, responsiveness to medical treatments [Time Frame: 2 years]
Secondary Outcome(s)
Secondary ID(s)
SCMCI082455CTIL
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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