Relationship of Peripheral Inflammatory and Neuroprotective Biomarkers With Response to Intermittent Theta Burst Stimulation in Treatment-Resistant Depression
- NCT ID
- NCT07673913
- Registry status
- Recruiting
- Study type
- Not specified in the registry data
- Phase
- Not applicable
- Sponsor
- Gulhane Training and Research Hospital
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 100 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- Yes
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria
Treatment-Resistant Depression Group:
Age between 18 and 55 years. Male or female participants. Diagnosis of Major Depressive Disorder according to DSM-5-TR criteria. Inadequate response to at least two antidepressant treatments administered at adequate doses and durations.
Eligible for transcranial magnetic stimulation (TMS) treatment. Able and willing to provide written informed consent. Able to complete neuropsychological assessments. Able to attend study visits and complete the treatment protocol.
Healthy Control Group:
Age between 18 and 55 years. Male or female participants. No current DSM-5-TR psychiatric disorder. Able and willing to provide written informed consent. Able to complete neuropsychological assessments.
Exclusion Criteria
Schizophrenia, bipolar disorder, organic mental disorders, or other major psychiatric disorders.
History of epilepsy, brain tumor, severe head trauma, or significant neurological disease.
Any contraindication to TMS. Presence of intracranial metal implants, cardiac pacemakers, cochlear implants, or other incompatible implanted devices.
Active infection. Autoimmune disease or chronic inflammatory disease. Electroconvulsive therapy, deep brain stimulation, or vagus nerve stimulation within the previous 5 years.
Previous intravenous or intranasal ketamine treatment. Pregnancy or breastfeeding. Active alcohol or substance use disorder. Inability to comply with study procedures. Inability to tolerate the iTBS protocol. Withdrawal of informed consent at any stage of the study.
Study locations
2 study locations are listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Turkey (Türkiye)
- Ankara, Turkey (Türkiye): 1
Sample of listed locations
- Gulhane Training and Research Hospital — Ankara, Ankara, 06000, Turkey (Türkiye) — Site recruitment status not specified in the registry data
- Gulhane Training and Research Hospital — Ankara, 06000, Turkey (Türkiye) — Site recruitment status not specified in the registry data
Study details
- Start date
- September 1, 2026
- Primary completion date
- September 1, 2027
- First posted
- June 29, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07673913
- Registry last updated
- September 14, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT07673913 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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