NCT07045142RecruitingPhase 3
Metformin Alleviates Abnormal Glucose Metabolism Induced by Statins in Schizophrenia Patients
Metformin Alleviates Abnormal Glucose Metabolism Induced by Statins in Schizophrenia Patients: A Randomized, Double-Blind, Placebo-Controlled Multicenter Clinical Study
Source: ClinicalTrials.gov · Last updated 3 Aug 2026
Brief summary (registry, in English)
Schizophrenia is a severe mental illness associated with significant morbidity and disability. Patients often experience metabolic side effects from antipsychotic medications, including weight gain and dyslipidemia. Statins, commonly used to manage dyslipidemia, can lower cholesterol levels but may increase the risk of new-onset diabetes. This study aims to investigate how atorvastatin affects glucose metabolism in schizophrenia patients and assess whether metformin can help improve these metabolic issues. The investigators will include 200 patients with dyslipidemia from the Second Xiangya Hospital and other sites, randomly assigning them to receive either atorvastatin with metformin or atorvastatin with placebo over six months. Key goals include evaluating the impact of atorvastatin on insulin resistance and blood glucose levels and determining the effectiveness of metformin in mitigating glucose metabolism abnormalities while managing lipid levels. Understanding these interactions will help improve treatment strategies for schizophrenia patients, potentially lowering their risk of cardiovascular diseases and diabetes and enhancing overall health outcomes.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 400 (estimated)
- First submitted
- 22 Jun 2025
- Start date
- 1 Jul 2025
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- Central South University
- Diseases
- Schizophrenia
- NCT number
- NCT07045142
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 400
- From 1 Jul 2025 to the primary completion date, 31 Dec 2027
- 8 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with a prior diagnosis of diabetes or complications such as diabetic ketoacidosis;
Lab values
- Patients with liver or kidney dysfunction, indicated by aspartate aminotransferase (AST), alanine aminotransferase (ALT), or gamma-glutamyl transferase (GGT) levels exceeding twice the normal limits, and/or creatinine levels exceeding 1.2 times the upper limit of the reference range or greater than 2 mg/dL, or deemed by the investigator to have liver and/or kidney impairment that warrants exclusion from the study;
- Patients with severe gastrointestinal, respiratory, endocrine, hematologic diseases, or metabolic absorption disorders: including but not limited to poorly controlled diabetes, severe acute systemic infections or immunological diseases, ischemic heart disease, cerebrovascular accidents within the past year, history of prolonged QT interval, active hepatitis B virus, chronic active hepatitis C, and malabsorption syndromes;
- Clinically significant abnormal ECG findings at screening that the investigator deems unsuitable for inclusion, such as male QTc interval \> 470 ms, female QTc interval \> 480 ms;
Other
- Pregnant or nursing women.
Who the study is looking for
- Aged between 18 and 65 years, regardless of gender, and meets the diagnostic criteria for schizophrenia according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5);
- Symptoms and medication regimen stable for more than 3 months, with the allowance of up to two antipsychotic medications in combination (concurrent use of antidepressants, anxiolytics, and mood stabilizers is permitted);
- Temporary use of benzodiazepines is allowed;
- Meets at least one of the following conditions: fasting total cholesterol (TC) ≥ 5.2 mmol/L; fasting triglycerides (TG) ≥ 1.7 mmol/L; fasting low-density lipoprotein cholesterol (LDL-C) ≥ 3.4 mmol/L;
- Two fasting blood glucose (FPG) tests must be \< 6.1 mmol/L (with an interval of 1-4 weeks);
- It is anticipated that there will be no issues related to relocation, transportation difficulties, or access to medical care throughout the study;
- Informed consent must be obtained from the patient and their guardian, and a consent form must be signed.
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (8)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Mental Health Institute of Second Xiangya Hospital,CSU Coordinator of this site? Confirm its status | Changsha | China | Recruiting |
| The Third Hospital of Changsha County Coordinator of this site? Confirm its status | Changsha | China | Active, not recruiting |
| The Second People's Hospital of Dali Bai Autonomous Prefecture Coordinator of this site? Confirm its status | Dali | China | Completed |
| Xiangshan County Traditional Chinese Medicine Hospital Medical and Health Group Three Hospitals District Coordinator of this site? Confirm its status | Xiangshan | China | Active, not recruiting |
| Yueyang Rehabilitation Hospital Coordinator of this site? Confirm its status | Yueyang | China | Recruiting |
| Junshan District Psychiatric Rehabilitation Hospital Coordinator of this site? Confirm its status | Yueyang | China | Active, not recruiting |
| The Second People's Hospital of Xiangyin County Coordinator of this site? Confirm its status | Yueyang | China | Active, not recruiting |
| Zhumadian Second People's Hospital Coordinator of this site? Confirm its status | Zhumadian | China | Active, not recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.