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Clinical Trial Details

Trial ID: L4097
Source ID: NCT04917458
Associated Drug: Cholecalciferol 4000 Iu Oral Capsule, Liquid Filled
Title: Cholecalciferol on Depressive Symptoms in Type 2 Diabetes Mellitus Patients
Acronym:
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Diabetes Mellitus, Type 2|Depressive Symptoms
Interventions: DRUG: Cholecalciferol 4000 IU Oral Capsule, Liquid Filled|DRUG: Placebo
Outcome Measures: Primary: Evaluating the effects of cholecalciferol for depression symptoms with BDI II score, Improvement rate on days 90 (end of study) as defined by a proportion of subjects with category of BDI II score below 13. The BDI II scale was a subjective measurement of depressive symptoms. Interpretation of BDI II were 0-13 for minimal depression, 14-19 for mild depression, 20-28 for moderate depression, and 29-63 for major depression. Cholecalciferol with doses of 4000 IU a day expected to demote BDI II scale or depressive symptoms in participants., 90 days | Secondary: Evaluating the effects of cholecalciferol against neuroplasticity (NT-3), NT-3 concentration (pg/ml) in the sample was determined by comparing the sample against the standard curve. Some studies have shown that neurotrophin-3 (NT-3 pg/ml) levels decreased in depression. Thus, cholecalciferol (for doses of 4000 IU a day) with expected could increase NT-3 pg/ml plasm levels. Furthermore, the enhancement of NT-3 pg/ml concentrates expected to had correlated with scale BDI II improvement., 30 days|Evaluating the effects of cholecalciferol against serotonin, Studies have shown that serotonin (ng/mL) in depressive patients had lower levels than patient without depressive syndrome. The serotonin levels were measured by the ELISA method. Cholecalciferol expected could increase levels of serotonin concentration (ng/mL) significantly 2-3 times after administrated., 30 days|Evaluating the effects of cholecalciferol against C-Peptide, C-peptide hormone is an indicator of insulin secretion. Specifically, a c-peptide level of less than 0.2 nmol/l is associated with a diagnosis of type 1 diabetes mellitus. C-peptide measured using ELISA at a minimal room temperature for 24 hours. Cholecalciferol expected could improve C-peptide levels concentration in type 2 Diabetes Mellitus., 30 days
Sponsor/Collaborators: Sponsor: Indonesia University
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 90
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: FACTORIAL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2021-01-18
Completion Date: 2021-10
Results First Posted:
Last Update Posted: 2021-06-08
Locations: Cipto Mangunkusumo National General Hospital, Jakarta Pusat, DKI Jakarta, 10430, Indonesia
URL: https://clinicaltrials.gov/show/NCT04917458