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Biomarkers of Antidepressant Response and Suicidal Events in Depressed Youth

Biomarkers of Antidepressant Response and Suicidal Events in Depressed Youth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03547219
Enrollment
152
Registered
2018-06-06
Start date
2015-08-05
Completion date
2018-08-02
Last updated
2019-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescent, Depression

Keywords

Depression, Adolescent, Biomarker, Inflammation, Brain-derived neurotrophic factor (BDNF), Functional MRI, Antidepressant, Machine learning

Brief summary

The aims of this study are to (1) identify inflammatory/neurotrophic and neurodevelopmental markers that predict antidepressant response and suicidal risk in depressed youth and (2) predict their treatment response and the occurrence of suicidal events at the individual level using machine learning approach.

Interventions

DRUGEscitalopram

Sponsors

National Research Foundation of Korea
CollaboratorOTHER
Seoul National University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* clinical diagnosis of major depressive disorder(MDD) according to criteria of Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) * current episode at least 4 weeks in duration at baseline * with a score of at least 40 on the Children's Depression Rating Scale-Revised (CDRS-R), and CGI-Severity ≥4 at baseline

Exclusion criteria

* intelligence quotient (IQ) lower than 70 * psychotic features or first-degree relatives with a history of bipolar I disorder * alcohol or substance abuse within the past 6 months * history of schizophrenia, bipolar disorder, eating disorder, or autism * history of neurological diseases including convulsive disorders or brain damage * concurrent medications with psychotropic effects (other than stimulants for ADHD) * chronic medical conditions (e.g., asthma, inflammatory bowel disease, diabetes) and/or chronic medication with psychotropic effects (e.g., anticonvulsants) or chronic use of NSAIDS or other drugs with known impact on inflammatory pathways.

Design outcomes

Primary

MeasureTime frameDescription
the change from baseline in CDRS-R at week 8 or upon terminationbaseline and 8 weeks or upon terminationThe Children's Depression Rating Scale-Revised (CDRS-R) is a clinician-rated scale to measure the severity of depression of children and adolescents. The CDRS-R consists of 17 items. Depression symptoms are rated on a 5-point scale from 1 to 5 for sleep, appetite, and tempo of speech items and a 7-point scale from 1 to 7 for remaining 14 items. The total score ranges form 17 (normal) to 113 (severe depression). Change from baseline CDRS-R at 8 weeks or upon termination was calculated as baseline minus 8 weeks in the adjusted CDRS-R total score (CDRS-R total minus 17, the minimum possible total score).

Secondary

MeasureTime frameDescription
CGI-I at 8 weeks or upon terminationbaseline and 8 weeks or upon terminationThe Clinical Global Impression - Improvement scale (CGI-I) is a 7 point scale that requires the clinician to assess how much the patient's illness has improved or worsened relative to a baseline state at the beginning of the intervention. and rated as: 1=very much improved; 2= much improved; 3=minimally improved; 4=no change from baseline; 5=minimally worse; 6=much worse; 7=very much worse since the initiation of treatment. CGI-I was measured at 8 weeks or upon termination

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026