Status:

COMPLETED

A 6-month Study to Evaluate Sulforaphane Effects in Schizophrenia Patients

Lead Sponsor:

Central South University

Conditions:

Schizophrenia

Eligibility:

All Genders

18-50 years

Phase:

PHASE2

Brief Summary

The goal of the study is to investigate whether adding sulforaphane will benefit the negative symptoms and cognitive function in individuals who have schizophrenia. This study will compare the sulfor...

Detailed Description

This study will be carried out in The Third Jiangyin Hospital in China and total of 120 schizophrenia patients with one negative symptom item score of PANSS≥3 will be enrolled into the study. Individu...

Eligibility Criteria

Inclusion

  • Meet The Diagnostic and Statistical Manual (DSM-5) diagnostic criteria for schizophrenia;
  • First onset or duration of illness less than 30 years with current symptoms in a stable condition;
  • Male and female aged 18 to 50 years;
  • Total score greater than or equal to 20 on the sum of the seven items constituting the Positive and Negative Syndrome Scale (PANSS) negative symptoms; an item of PANSS negative symptoms \>3 scores;
  • Signed the study consent for participation.

Exclusion

  • has a history of substance dependence or abuse or whose symptoms are caused by other diagnosable mental disorders;
  • has a history of traumatic brain injury, seizures, or other known neurological diseases of the central nervous system;
  • taking antidepressants, stimulants, mood stabilizers, or received modified electroconvulsive therapy (MECT) or rTMS during the past three months;
  • having current suicidal or homicidal thoughts or any safety concern by research staff that cannot be managed during the trial;
  • taking dementia-related drugs, minocycline, and other drugs that may affect cognitive function;
  • Laboratory tests indicated significant abnormalities in blood routine, liver and kidney function, or other metabolic results;
  • pregnant or lactating women.

Key Trial Info

Start Date :

August 31 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 12 2022

Estimated Enrollment :

125 Patients enrolled

Trial Details

Trial ID

NCT04521868

Start Date

August 31 2020

End Date

August 12 2022

Last Update

April 26 2023

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Second Xiangya Hospital

Changsha, Hunan, China, 410008