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WithdrawnNCT00534898

Bexarotene and Fenretinide as Addition to Antipsychotic Treatment in Schizophrenia Patients

This study evaluates the effectiveness of Bexarotene for people with schizophrenia.

Medication studyAges 18–60Israel
The study in practice

Understand this study

What is this study about?

This study evaluates the effectiveness of Bexarotene for people with schizophrenia.

Who could participate?

This study is for people with schizophrenia. Listed age limits: 18 years to 60 years. Other eligibility criteria apply.

Listed locations
Be'er Sheva, HaderaSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateNot clearly listed
Recruitment status
Withdrawn
Enrollment listed in the registry
Not clearly listed
Sponsor
Beersheva Mental Health Center
Sponsor type
Hospital / academic medical center
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
Israel
Age range
From 18 Years to 60 Years
Official registry ID
NCT00534898
Official title
Show the full official title

Comparison Efficacy of Bexarotene and Fenretinide as Addition to Antipsychotic Treatment in Schizophrenia Patients: Double-blind Placebo Controlled Study

Recruitment & locations

Withdrawn

Be'er Sheva, Hadera

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FAQ

Questions about this study

What is this study about?

This study evaluates the effectiveness of Bexarotene for people with schizophrenia.

Who is behind this study?

The study sponsor is Beersheva Mental Health Center, a hospital or academic medical center.

Does this study involve medication?

Yes. The study involves medication, including Bexarotene, Fenretinide and Placebo.

Who can participate?

This study is for people with schizophrenia. Listed age limits: 18 years to 60 years. Other eligibility criteria apply.

Is this study still recruiting?

The registry lists this study as withdrawn.

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