The Effect of Gliatamin (Chonline Alphoscerate) on Depressive Mood in Type 2 Diabetes Patients
Launched by YONSEI UNIVERSITY · Feb 16, 2017
Trial Information
Current as of November 10, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the effects of a medication called Gliatamin (choline alphoscerate) on improving depressive moods in patients with type 2 diabetes. Researchers believe that by helping to reduce feelings of depression, the medication might also enhance the overall quality of life and better manage blood sugar levels in these patients. The study is currently recruiting participants, and anyone aged 50 and older with type 2 diabetes and certain levels of depression may be eligible to join.
To participate, individuals must have their diabetes under control and meet specific criteria related to their mental health. Participants will be asked to understand the study process and will need to give written consent to join. Throughout the trial, participants can expect close monitoring and support as they explore the potential benefits of this treatment. It's important to note that certain health conditions or current treatments may prevent some people from being eligible, so discussing personal health history with the study team is crucial.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Type 2 diabetic patients
- • Age ≥ 50
- • Glycemic control: HbA1c ≤ 10.0%
- • 10 ≤ Beck Depression Inventory (BDI) \<30 points
- • Participants who can undergo contraception in case of being in childbearing period
- • Understands the study procedure, alternatives, and risks and voluntarily agrees to participate by giving written informed concent
- Exclusion Criteria:
- • Type 1 diabetes, Secondary diabetes, gestational diabetes
- • Ongoing dementia treatment or anti-depressive disorder medication
- • Uncontrolled psychiatric disorder
- • BDI ≥ 30 points
- • Heavy alcoholics
- • Underlying chronic liver disease (hemochromatosis, liver cell carcinoma, autoimmune liver disease, liver cirrhosis, chronic viral hepatitis)
- • Allergy or hypersensitivity to target medication or any of its components
- • Renal failure, moderate or severe renal impairment (estimated glomerular filtration rate \< 30 mL/min/1.73 m2), or ongoing dialysis
- • Abnormal liver function (AST/ALT \> x3 upper normal limit)
- • History of alcohol or drug abuse in the previous 3 months
- • Premenopausal women who are nursing or pregnant
- • Human immunodeficiency virus (HIV) or human immunodeficiency virus (AIDS)
- • chronic pancreatitis or pancreatic cancer
About Yonsei University
Yonsei University, a prestigious institution located in South Korea, is renowned for its commitment to advancing medical research and education. As a clinical trial sponsor, Yonsei University leverages its extensive expertise and innovative approaches in various fields of medicine to conduct rigorous clinical trials aimed at improving patient outcomes and advancing healthcare solutions. The university's robust infrastructure, multidisciplinary collaboration, and adherence to ethical standards ensure the integrity and reliability of its research initiatives, making it a key player in the global clinical research landscape.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Seoul, Korea, Republic Of
Seoul, Korea, Republic Of
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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