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Study of the effect of benzoic acid on glutamic acid

Effects of sodium benzoate on glutamate and glutathione levels in patients with treatment-resistant schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031200050
Enrollment
25
Registered
2020-06-12
Start date
2020-06-12
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizophrenia Schizophrenia

Interventions

Administer sodium benzoate (2 g / day) and obs erve for 6 weeks.

Sponsors

Iwata Yusuke
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) DSM-V diagnosis of schizophrenia or schizoaffective disorder. 2) Age 18 to 65 years. 3) History of failure (score of 4 or more on 2 PANSS positive symptom items and CGI-Severity score of 4 or more) to respond to two or more different kinds of antipsychotics, each attaining a chlorpromazine daily dose of 400 mg or more for a duration 4 or more consecutive weeks. 4) On the same antipsychotic in the last 4 weeks before the inclusion. 5) Subject who provided written informed consent for research.

Exclusion criteria

Exclusion criteria: 1) Substance abuse or dependence (within past six months), excluding nicotine and caffeine. 2) Metal implants or a pace-maker that would preclude the MRI scan. 3) History of head trauma resulting in loss of consciousness > 30 minutes that required medical attention. 4) Unstable physical illness or significant neurological disorder including a seizure disorder. 5) Refusal to give consent to investigator to communicate with physician of record for the entire duration of the study. 6) Psychiatric concerns raised by the physician of record regarding participation in the study. 7) Currently taking clozapine 8) Currently taking medications that may directly impact the glutamatergic system (i.e. lamotrigine, topiramate, memantine)

Design outcomes

Primary

MeasureTime frame
Change in the brain glutamate and glutathione levels before and after sodium benzoate administration.

Secondary

MeasureTime frame
1) Correlation between glutamate and glutathion e concentrations in the brain and the total points of "Positive and Negative Syndrome Scale (PANSS)" at the baseline and 6 weeks after administarati on 2) Correlation between glutamate and glutathion e concentrations in the brain at the baseline and t he total points of "Positive and Negative Syndrom e Scale (PANSS)" 3) Changes in the glutamate levels in the blood after 6 weeks of sodium benzoate intake

Contacts

Public ContactYusuke Iwata

Yamanshi University Hospital

yiwata@yamanashi.ac.jp+81-55-273-9847

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026