Luteolin for the Treatment of People With Schizophrenia

About

Brief Summary

Luteolin is a natural product found in foods such as celery, green pepper, parsley, and chamomile tea. It has been found to have anti-cancer, anti-oxidant, and anti-inflammatory properties. The purpose of this study is to determine if luteolin helps improve symptoms of schizophrenia.

Primary Purpose

Treatment

Study Type

Interventional

Phase

Phase IV

Eligibility

Gender

All

Healthy Volunteers

Minimum Age

18 Years

Maximum Age

60 Years

Inclusion Criteria:

Either male or female of any race
Age is 18-60 years old
Meets DSM-5 criteria for schizophrenia or schizoaffective disorder
Positive and Negative Syndrome Scale (PANSS) total score of 75 or more OR a Clinical Global Impression severity of illness item score of 4 or more
Clinically stable
Treated with the same antipsychotic for at least 60 days and have received a constant therapeutic dose for at least 30 days prior to study entry
Able to participate in the informed consent process and provide voluntary informed consent

Exclusion Criteria:

Meets DSM-5 criteria for alcohol or substance misuse (except caffeine and nicotine) within the last 6 months; or a positive baseline urine drug screen. Participants who meet DSM-5 criteria for marijuana misuse - mild will be included in the study
A current infection, including HIV and Hepatitis C; or an organic brain disorder or medical condition, whose pathology or treatment could alter the presentation or treatment of schizophrenia or significantly increase the risk associated with the proposed treatment protocol
Currently taking immunosuppressive medications (e.g. oral scheduled corticosteroids, chemotherapy or transplantation or HIV/AIDs associated drugs); or anti-inflammatory medications, including NSAIDs (e.g. ibuprofen, celecoxib, or naproxen) or aspirin > 81 mg on a daily basis. The use of PRN anti-inflammatory agents will be allowed.
Female participants who are pregnant or nursing

Join this Trial

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