Pyrroloquinoline Quinone for Negative and Cognitive Symptoms in Chronic Schizophrenia
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.
Pyrroloquinoline quinone (PQQ)
+ placebo (dietary fiber)
Mental Disorders+5
+ Nervous System Diseases
+ Neurologic Manifestations
Treatment Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.70 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives