Antipsychotic Effects of Probiotics and Prebiotics on Patients With Schizophrenia

Schizophrenia Clinical Trial

Official title:

A Prospective, Randomized, Controlled Multicenter Trial of Probiotics and Prebiotics to Improve the Efficacy of Antipsychotics in Patients With Schizophrenia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04291469
• Other study ID #: XJTU1AF-CRF-2019-003
• Status: Recruiting
• Phase: N/A
• Start date: March 3, 2022
• Est. completion date: December 2022

Study information

• Verified date: April 2022
• Source: First Affiliated Hospital Xi'an Jiaotong University
• Contact: YingYing Dong, M.D.
• Phone: 0086-13992808564
• Email: 406022725[@]qq.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this study, investigators will evaluate the efficacy and related mechanism of probiotics and prebiotics as an add-on treatment in improving the antipsychotic induced psychotic syndrome, the cognitive impairment, gastrointestinal function, and metabolic disorders in schizophrenia patients, through genotype identification, psychopathology, neuropsychology, biochemical evaluation and other methods.

Description:

The study will recruit 210 schizophrenia patients who meet the criteria of DSM-4, and then randomized to 3 groups: control group, probiotics group and prebiotics group for a 14-weeks clinical trail and 12-weeks follow-up period. In addition to probiotics, prebiotic or maltodextrin interventions, in the meantime, all participants will also use one of the prescribed antipsychotics medications. Clinical efficacy and safety assessment will be done at baseline, clinical trail and follow-up period. The specific aims are to evaluate these tips: 1) psychotic syndrome; 2) cognition; 3) Gastrointestinal function; 4) inflammatory and metabolic related markers. Psychotic syndrome will be measured by the Positive and Negative Syndrome Scale. Cognitive function will be assessed by the MATRICS Consensus Cognitive Battery. Gastrointestinal function will be assessed by gastrointestinal symptom assessment scale (GSRS). Biological samples also will be collected, and stored to research Intestinal inflammation, intestinal permeability, intestinal flora and other indicators.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: December 2022
• Est. primary completion date: December 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Meet the Diagnostic and Statistical Manual (DSM-V) diagnostic criteria for schizophrenia
• Duration of illness 5 years, Subjects are currently receiving first-line recommended antipsychotic medication
• The total PANSS score =60, containing at least three positive or negative items with scores of 3 or more at screening
• Junior high school or above
• Capacity for written informed consent.

Exclusion Criteria:

• Pregnant or lactating women
• Any clinically significant or unstable medical disorder as determined by the investigators, including congestive heart failure, abnormal liver function, renal failure, immunodeficiency diseases, cancer, or gastrointestinal diseases ( inflammatory bowel disease or celiac disease, except functional constipation)
• Subjects had acute or chronic infections or are taking anti-inflammatory drugs and cortisol hormones. Receipt of antibiotic medication within the previous 1 month.
• Other neuropsychiatric disorders (organic diseases of the central nervous system, a mental disorder caused by a physical disease or psychoactive substance, mental retardation).
• Having history of substance dependence or abuse,including alcohol
• BMI is not within the normal range (18.5 to 23.9)

Related Conditions & MeSH terms

• Schizophrenia

Intervention

Drug:
• Probiotics(Live combined bifidobacteria, lactobacillus and maltodextrin tables)
The probiotic compound will consist of tables containing approximately 10^9 colony forming units of the probiotic organisms, Lactobacillus and Bifidobacteria lactis strain,mixed maltodextrin(oral, daily for 14 weeks).

Dietary Supplement:
• Prebiotics (Combined inulin and maltodextrin tables)
The prebiotic compound will consist of tables containing inulin and maltodextrin (oral,daily for 14 weeks)
• maltodextrin
Maltodextrin tables (oral,daily for 14 weeks)

Locations

Country	Name	City	State
China	First Affiliated Hospital of Xi'an Jiao tong University	Xi'an	Shanxi

Sponsors (5)

Lead Sponsor	Collaborator
First Affiliated Hospital Xi'an Jiaotong University	BaoJi Rehabilitation Hospital, HanZhong Psychiatric Hospital, WeiNan Psychiatry Hospital, Xiangyang Central Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Positive and Negative Syndrome Scale (PANSS) Score from week0 to week26	The complete PANSS contains ratings for 30 symptoms, including 7 positive symptoms, 7 negative symptoms, and 16 general psychiatric symptoms. The clinical efficacy was evaluated by its score reduction rate, with the total score reduction rate =75% as recovery, 50% ~ 74% as significant improvement, 25% ~ 49% as improvement, and <25% as invalid. improvement, significant improvement and recovery add up to apparent effect.	26weeks(week0 to week26)
Secondary	Change in MATRICS Consensus Cognitive Battery(MCCB) Score from week1 to week26	Change in the Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery (MCCB) score from the start of Trial period to the end of the follow-up phase; Cognitive performance is measured by the MATRICS Consensus Cognitive Battery composite score in participants.	week26(week1 to week26 )
Secondary	Gastrointestinal symptom rating scale (GSRS)	Gastrointestinal function will be assessed during the screening stage,week 4, week 8, week 12, week 14 of treatment stage and once every 4 weeks of follow-up stage through Gastrointestinal symptom rating scale (GSRS); The score reduction of GSRS=25% was associated with improvement in gastrointestinal function.	week26 (week1 to week26)
Secondary	Serum inflammatory factors-TH-1	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines --TH-1	week26(week1 to week26)
Secondary	Serum inflammatory factors-TH-2	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines--TH-2	week26(week1 to week26)
Secondary	Serum inflammatory factors-TH-17	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines--TH-17	week26(week1 to week26)
Secondary	Serum inflammatory factors-Interleukin-1	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines--Interleukin-1	week26(week1 to week26)
Secondary	Serum inflammatory factors-Interleukin-2	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines --Interleukin-2	week26(week1 to week26)
Secondary	Serum inflammatory factors-Interleukin-6	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines --Interleukin-6	week26(week1 to week26)
Secondary	Serum inflammatory factors-Interleukin-10	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines --Interleukin-10	week26(week1 to week26)
Secondary	Serum inflammatory factors-Interleukin-17	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines --Interleukin-17	week26(week1 to week26)
Secondary	Serum inflammatory factors-TNF-a	Change of intestinal inflammation will be assessed during the the double-blind phase, including serum inflammatory cytokines --TNF-a(tumor necrosis factor-a,interferon).	week26(week1 to week26)
Secondary	Fecal intestinal flora	The number of lactobacillus and bifidobacterium flora will be assessed; The species and abundance of intestinal flora were identified by 16SrRNA.	week26 (week1 to week26)
Secondary	Serum intestinal permeability index-FABP2	Change of Serum intestinal permeability index will be assessed during the the double-blind phase- FABP2	week26(week1 to week26)
Secondary	Serum intestinal permeability index-sCD14	Change of Serum intestinal permeability index will be assessed during the the double-blind phase-sCD14	week26(week1 to week26)
Secondary	Serum intestinal permeability index-LBP	Change of Serum intestinal permeability index will be assessed during the the double-blind phase-LBP	week26(week1 to week26)