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Pyrroloquinoline Quinone for Negative and Cognitive Symptoms in Chronic Schizophrenia

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Study Aim

This study aims to evaluate the effects of Pyrroloquinoline Quinone on cognitive and negative symptoms in individuals with chronic schizophrenia, by observing changes in scores of MCCB and PANSS negative subscale from the baseline to the first post-treatment measurement.

What is being tested

Pyrroloquinoline quinone (PQQ)

+ placebo (dietary fiber)

Dietary Supplement
Who is being recruted

Mental Disorders+5

+ Nervous System Diseases

+ Neurologic Manifestations

From 18 to 50 Years
+15 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-Controlled
Interventional
Study Start: February 2026
See protocol details

Summary

Principal SponsorTianjin Anding Hospital
Study ContactDaxiang Medical Ethics Committee of Tianjin Anding Hospital
Last updated: February 11, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 15, 2026

Actual date on which the first participant was enrolled.

Schizophrenia is a mental health condition that comes with various symptoms, including negative symptoms and cognitive issues. Some studies suggest that addressing problems like mitochondrial dysfunction, oxidative stress, and inflammatory responses could help ease these symptoms, but results vary. This study focuses on a substance called Pyrroloquinoline quinone (PQQ) and its potential to reduce negative symptoms and improve cognitive function in individuals with chronic schizophrenia. The goal is to understand if PQQ could be a helpful addition to current treatments, potentially enhancing the quality of care for those living with this condition. During this study, participants diagnosed with chronic schizophrenia will be randomly assigned to receive either PQQ or a placebo. The study will track changes in symptom severity from the start to the end of the treatment, and for eight weeks after. To measure these changes, researchers will use questionnaires and neuroimaging techniques, such as resting-state scans and multimodal tasks. These tools help assess functional connectivity and activation in specific brain regions. Safety is a priority, and any adverse events will be closely monitored. The study also aims to understand if factors like age and gender could influence the effects of PQQ.

Official TitleThe Efficacy and Safety of Pyrroloquinoline Quinone add-on Treatment for Negative and Cognitive Symptoms in Chronic Schizophrenia
Principal SponsorTianjin Anding Hospital
Study ContactDaxiang Medical Ethics Committee of Tianjin Anding Hospital
Last updated: February 11, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

70 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 50 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Mental DisordersNervous System DiseasesNeurologic ManifestationsSchizophreniaSigns and SymptomsPathological Conditions, Signs and SymptomsNeurobehavioral ManifestationsSchizophrenia Spectrum and Other Psychotic Disorders

Criteria

6 inclusion criteria required to participate
Participants are required to complete a comprehensive safety questionnaire addressing potential risks associated with exposure to a 3-Tesla magnetic field and the MRI environment

A Positive and Negative Syndrome Scale (PANSS) total scores of ≥ 60 (indicating an active phase of the illness)

A PANSS negative subscale scores of ≥ 20

A duration of illness of at least 2 years (indicating chronic schizophrenia)

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9 exclusion criteria prevent from participating
A history of possible intraocular metallic foreign bodies due to manual labor without appropriate eye protection

Claustrophobia

Unwillingness to be informed of any incidental structural brain abnormalities detected during the scan

Patients with comorbid psychiatric disorders as defined by the DSM-5, such as substance abuse or dependence (excluding nicotine), or intellectual disability (IQ < 70)

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental

Group II

Placebo

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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