The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome

NCT ID: NCT00768820

Last Updated: 2024-05-07

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

Clinical Phase

PHASE4

Total Enrollment

400 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-05-31

Study Completion Date

2024-08-31

Brief Summary

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The purpose of this study is to investigate 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

Detailed Description

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Conditions

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Velocardiofacial Syndrome Williams Syndrome Fragile X Syndrome

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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1

Group Type EXPERIMENTAL

methylphenidate, fluoxetin, risperidone

Intervention Type DRUG

first cognitive evaluation without methylphenidate,second cognitive evaluation with methylphenidate

Interventions

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methylphenidate, fluoxetin, risperidone

first cognitive evaluation without methylphenidate,second cognitive evaluation with methylphenidate

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* chromosomal deletion proven by FISH examination
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Chaim Sheba Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Prof. Doron Gothelf

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Schneider Children's Mediac Center of Israel

Petah Tikva, , Israel

Site Status RECRUITING

Countries

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Israel

Central Contacts

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Doron Gothelf, MD

Role: CONTACT

972-03-5302663

Facility Contacts

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Doron Gothelf, MD

Role: primary

972-03-5302663

Other Identifiers

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SCMCI082455CTIL

Identifier Type: -

Identifier Source: org_study_id

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