Yonsei University College of Medicine, Department of Internal Medicine, Division of Endocrinology, Severance Hospital, Diabetes Center
Seoul, 03722, South Korea
Location status: Recruiting
NCT Number: NCT03059069
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.
Interested in participating?
Request Info50 year and older
All sexes
Interventional
Phase 4
Seoul, 03722, South Korea
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients treated with Chonline Alphoscerate as add on therapy to their medication
Other names: Gliatamin
Patients maintain their medication with either Gliatamin or placebo for 6 months.
Time frame: 6 months after the treatment
The HDRS will be scored by face-to-face interview.
Time frame: 6 months after the treatment
MMSE questionnaire will be checked by careful interview and self-reported.
Time frame: 6 months after the treatment
fasting glucose (mg/dL)
Time frame: 6 months after the treatment
postprandial 2h glucose (mg/dL)
Time frame: 6 months after the treatment
fasting insulin (uIU/mL)
Time frame: 6 months after the treatment
homeostasis model assessment for insulin resistance (mg/dL•uIU/mL)
Time frame: 6 months after the treatment
aspartate aminotransferase (IU/L)
Time frame: 6 months after the treatment
alanine aminotransferase (IU/L)
Time frame: 6 months after the treatment
glycated hemoglobin (%)
Time frame: 6 months after the treatment
glycoalbumin (%)
Time frame: 6 months after the treatment
triglyceride (mg/dL)
Time frame: 6 months after the treatment
low-density lipoprotein (mg/dL)
Time frame: 6 months after the treatment
high-density lipoprotein (mg/dL)
Contact information is provided by the study sponsor or research team.
Yonsei University
Other
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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.