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The Relationship of EEG Microstate Parameters and Neuroinflammatory Biomarkers With Treatment Response in Patients With Treatment-Resistant Major Depressive Disorder Receiving Electroconvulsive Therapy

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

This study aims to investigate the neurophysiological and inflammatory changes associated with electroconvulsive therapy (ECT) in patients diagnosed with Major Depressive Disorder who are resistant to at least two antidepressant treatments, using microstate analysis derived from resting-state electroencephalography (EEG) recordings. Within this scope, EEG recordings obtained before and after ECT will be compared to determine the relationships between changes in microstate parameters and inflammatory marker levels, clinical variables, and psychometric scale scores reflecting clinical improvement. Peripheral blood samples collected from the same patient group will be analyzed for complete blood count parameters as well as levels of interleukin-1 alpha (IL-1α), interleukin-1 beta (IL-1β), interleukin-2 (IL-2), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), tumor necrosis factor-alpha (TNF-α), soluble glycoprotein 130 (sgp-130), soluble interleukin-6 receptor (sIL-6R), interferon gamma-induced protein 10 kDa (IP-10), and C-reactive protein (CRP). In addition, inflammatory indices, including the Neutrophil-to-Lymphocyte Ratio (NLR), Platelet-to-Lymphocyte Ratio (PLR), and Monocyte-to-Lymphocyte Ratio (MLR), will be calculated. The association between baseline levels of these biomarkers and treatment response will be evaluated. Moreover, changes in biomarker levels following ECT will be statistically examined in relation to clinical scale scores and EEG microstate parameters. Although microstate analysis and inflammatory biomarkers have each been extensively investigated in psychiatric disorders, studies evaluating these two biomarkers together, particularly with the inclusion of healthy control participants, remain limited. In this regard, the present study aims to evaluate the effects of ECT on patients with treatment-resistant depression using objective neurophysiological indicators, to contribute to the understanding of the pathophysiology of depression at the level of brain networks, and to provide a scientific basis for the development of personalized treatment approaches in the future.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: t
View:

⁃ Patient Group

• Age 18-60 years

• Diagnosis of Major Depressive Disorder, current major depressive episode, according to DSM-5 criteria.

• Clinical indication for electroconvulsive therapy (ECT).

• Ability to provide written informed consent.

• Willingness to participate in the study.

⁃ Healthy Control Group:

• Age ≥55 years.

• No current psychiatric disorder.

• No known neurological disorder.

• Good general physical health.

• No current use of medications known to affect EEG activity or inflammatory biomarkers significantly.

• Ability to provide written informed consent.

• Willingness to participate in the study.

Locations
Other Locations
Turkey
İstanbul University- Cerrahpasa, Cerrahpasa Medicine Faculty, Psychiatry Department
RECRUITING
Istanbul
Contact Information
Primary
Zeynep Özge Dagoglu Sarac, Dr
zod395@gmail.com
+905365942469
Backup
Yusuf Cicek, Dr
yusuf.cicek@iuc.edu.tr
+905349624762
Time Frame
Start Date: 2026-01-01
Estimated Completion Date: 2027-03
Participants
Target number of participants: 62
Treatments
Patients between 18 and 60 years of age diagnosed with Treatment Resistant Major Depressive Disorder
Healthy control
The healthy control group will consist of age- and sex-matched volunteers between 18 and 60 years of age who do not use any medication that may significantly influence EEG activity or inflammatory biomarkers, and who do not have a current neurological or psychiatric disorder. Healthy controls will also provide written informed consent before participation. EEG recordings will be obtained once and will serve as reference data for normal brain activity.
Related Therapeutic Areas
Sponsors
Leads: Istanbul University - Cerrahpasa

This content was sourced from clinicaltrials.gov