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NCT Number: NCT03059069

The Effect of Gliatamin (Chonline Alphoscerate) on Depressive Mood in Type 2 Diabetes Patients

The aim of this study is to investigate the effect of Gliatamin (chonline alphoscerate) on depressive mood in type 2 diabetes patients and demonstrate the impact of improved depressive mood could be influence the patient's quality of life and glycemic control.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Yonsei University College of Medicine, Department of Internal Medicine, Division of Endocrinology, Severance Hospital, Diabetes Center

Seoul, 03722, South Korea

Location status: Recruiting

Location contact

Bong Soo Cha, MD

CONTACT

[email protected]

+82-2-2228-1932

About this study

The prevalence of depressive disorder is higher in individuals with chronic diseases, and the screening and management of depression is emphasized. Diabetes mellitus (DM) is a class of chronic disease and the incidence of DM has been increasing. According to previous study, 31.1% of patients with DM accompanied with depressive disorders which was higher than that of subjects without DM. Furthermore, DM as well as depression is known for risk factor for dementia.

The choline metabolism involves in neuropathology of depressive disorders and individuals with depressive disorders showed the lower level of choline concentration. Choline alphoscerate is cholinergic precursor and showed the favorable clinical results in dementia management.

As pseudodementia can be presented as depressive disorder and choline alphoscerate would be an option for these cases. Therefore, the aim of this study is to investigate the effect of Gliatamin (chonline alphoscerate) on depressive mood in type 2 diabetes patients and demonstrate the impact of improved depressive mood could be influence the patient's quality of life and glycemic control.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Chonline Alphoscerate

Drug

Patients treated with Chonline Alphoscerate as add on therapy to their medication

Other names: Gliatamin

Placebo oral tablet

Drug

Patients maintain their medication with either Gliatamin or placebo for 6 months.

Primary outcomes

  1. changes in Hamilton Depression Rating Scale (HDRS)

    Time frame: 6 months after the treatment

    The HDRS will be scored by face-to-face interview.

Secondary outcomes

  1. changes in Mini-mental state examination (MMSE) score

    Time frame: 6 months after the treatment

    MMSE questionnaire will be checked by careful interview and self-reported.

  2. glucometabolic parameters

    Time frame: 6 months after the treatment

    fasting glucose (mg/dL)

  3. glucometabolic parameters

    Time frame: 6 months after the treatment

    postprandial 2h glucose (mg/dL)

  4. glucometabolic parameters

    Time frame: 6 months after the treatment

    fasting insulin (uIU/mL)

  5. glucometabolic parameters

    Time frame: 6 months after the treatment

    homeostasis model assessment for insulin resistance (mg/dL•uIU/mL)

  6. glucometabolic parameters

    Time frame: 6 months after the treatment

    aspartate aminotransferase (IU/L)

  7. glucometabolic parameters

    Time frame: 6 months after the treatment

    alanine aminotransferase (IU/L)

  8. glucometabolic parameters

    Time frame: 6 months after the treatment

    glycated hemoglobin (%)

  9. glucometabolic parameters

    Time frame: 6 months after the treatment

    glycoalbumin (%)

  10. glucometabolic parameters

    Time frame: 6 months after the treatment

    triglyceride (mg/dL)

  11. glucometabolic parameters

    Time frame: 6 months after the treatment

    low-density lipoprotein (mg/dL)

  12. glucometabolic parameters

    Time frame: 6 months after the treatment

    high-density lipoprotein (mg/dL)

Study contacts

Contact information is provided by the study sponsor or research team.

Bong-Soo Cha, MD, Ph.D

CONTACT

[email protected]

82-2-2228-5457

Sponsors and collaborators

Lead sponsor

Yonsei University

Other

Registry information

Important dates

Study start
2016
Primary completion
2025
Study completion
2025
First posted
Feb 23, 2017
Registry last updated
Feb 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.