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Recruiting Phase 4 NCT00768820

NCT00768820 The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome

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Clinical Trial Summary
NCT ID NCT00768820
Status Recruiting
Phase Phase 4
Sponsor The Chaim Sheba Medical Center
Condition Velocardiofacial Syndrome
Study Type INTERVENTIONAL
Enrollment 400 participants
Start Date 2001-05
Primary Completion 2027-08

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
methylphenidate, fluoxetin, risperidone

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 4 studies follow an already-approved treatment in real-world conditions to monitor long-term safety and effectiveness.

This trial targets 400 participants in total. It began in 2001-05 with a primary completion date of 2027-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Eligibility Criteria

Inclusion Criteria: * chromosomal deletion proven by FISH examination Exclusion Criteria:

Contact & Investigator

Central Contact

Doron Gothelf, MD

✉ gothelf@post.tau.ac.il

📞 972-03-5302663

Frequently Asked Questions

Who can join the NCT00768820 clinical trial?

This trial is open to participants of all sexes, studying Velocardiofacial Syndrome. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT00768820 trial and what does that mean for participants?

Phase 4 studies are conducted after a treatment has been approved. They monitor long-term safety and real-world effectiveness in a broader patient population.

Is NCT00768820 currently recruiting?

Yes, NCT00768820 is actively recruiting participants. Contact the research team at gothelf@post.tau.ac.il for enrollment information.

Where is the NCT00768820 trial being conducted?

This trial is being conducted at Petah Tikva, Israel.

Who is sponsoring the NCT00768820 clinical trial?

NCT00768820 is sponsored by The Chaim Sheba Medical Center. The trial plans to enroll 400 participants.

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