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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