EEG microstates of wakefulness and NREM sleep.
Verena Brodbeck, Alena Kuhn, Frederic von Wegner...
https://pubmed.ncbi.nlm.nih.gov/22658975/Actively Recruiting
Led by Istanbul University - Cerrahpasa · Updated on 2026-08-05
62
Participants Needed
1
Research Sites
12 weeks
Total Duration
Researchers are investigating the neurophysiological and inflammatory changes linked to electroconvulsive therapy ECT in adults with treatment-resistant Major Depressive Disorder who have not responded to at least two antidepressant treatments. The study aims to understand how ECT affects brain network activity using EEG microstate analysis and to explore relationships between brain activity changes, inflammatory markers, and clinical improvements. This work hopes to provide new insights into depression and help guide personalized treatments. Participants include adults aged 18 to 60 with treatment-resistant depression who will undergo ECT using a device called the Thymatron System IV under general anesthesia. Healthy volunteers matched by age and sex will also participate as controls. EEG recordings will be taken before ECT and at two points after treatment to analyze brain activity patterns. Blood samples will be collected before and after ECT to measure various inflammatory biomarkers and calculate inflammatory indices. During the study, participants will complete several clinical scales assessing depression, anxiety, and cognitive function at baseline and after treatment. EEG recordings involve resting-state measurements with eyes open and closed. The study will examine changes in EEG microstate parameters and inflammatory markers over time and their association with clinical outcomes. The total participation includes assessments before ECT, and follow-ups up to eight weeks after treatment ends.
CONDITIONS
EEG Microstate Parameters and Neuroinflammatory Biomarkers in Patients With Treatment-Resistant Major Depressive Disorder Receiving ECT
Z
Zeynep Özge Dagoglu Sarac, Dr
Y
Yusuf Cicek, Dr
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Istanbul University - Cerrahpasa
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Varies by patient based on clinical condition
Participants diagnosed with treatment-resistant depression receive electroconvulsive therapy according to their clinical needs, administered under general anesthesia using the Thymatron System IV device.
Multiple visits during treatment course
Duration - Up to 8 weeks after treatment completion
Participants undergo EEG recordings and clinical assessments before ECT, and again approximately 2 and 8 weeks after completing the ECT sessions. Blood samples are also collected at these times to measure inflammatory markers.
3 assessment visits including EEG and blood tests
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Lead Sponsor