[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100595970":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":21,"locations":27,"responsibleParty":50,"collaborators":20,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":62,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":20,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":75,"overallStatus":29,"whyStopped":20,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Gulhane Training and Research Hospital","OTHER_GOV",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Transcranial Magnetic Stimualtion Treatment Arm","EXPERIMENTAL","This arm includes participants diagnosed with treatment-resistant depression (TRD) who will receive transcranial magnetic stimulation (TMS) therapy. TMS will be delivered using the MagVenture™ X100™ device. The treatment protocol consists of 20 sessions over a 4-week period (5 sessions per week). Stimulation will target the left dorsolateral prefrontal cortex (DLPFC) using intermittent theta burst stimulation (iTBS). Motor threshold will be determined at baseline and reassessed weekly to calibrate stimulation intensity at 90% of the resting motor threshold.\n\nBlood samples will be collected from participants at two time points: prior to the first TMS session (pre-treatment) and following the final (20th) session (post-treatment). Proteomic and metabolomic analyses will be performed using high-resolution liquid chromatography-mass spectrometry (LC-MS). The goal is to identify differentially expressed proteins and metabolites associated with clinical response to TMS.",[13],"Device: TMS",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","TMS","Transcranial Magnetic Stimulation (TMS) is a non-invasive brain stimulation technique approved for the treatment of major depressive disorder (MDD), particularly in individuals with treatment-resistant depression (TRD). TMS targets the left dorsolateral prefrontal cortex (DLPFC), a brain region often underactive in depression, and modulates neural activity through magnetic pulses.\n\nThis study aims to evaluate the effects of TMS on plasma proteomic and metabolomic profiles in patients with TRD. Participants will undergo 20 sessions of intermittent theta burst stimulation (iTBS) over four weeks. Blood samples will be collected before and after treatment to identify molecular changes associated with clinical response. Healthy controls will provide single-time-point blood samples for baseline comparison. Findings may support the development of biomarker-based strategies for personalized treatment in psychiatry.",[9],null,[22],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},"BEYAZIT GARİP, Medical Doctor","CONTACT","+903123044512","beyazitgarip@gmail.com",[28,41],{"facility":5,"status":29,"city":30,"state":30,"zip":31,"country":32,"countryCode":20,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"RECRUITING","Ankara","06000","Turkey (Türkiye)",{"type":34,"coordinates":35},"Point",[36,37],32.85427,39.91987,{"lat":37,"lon":36},[40],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},{"facility":5,"status":29,"city":30,"state":30,"zip":42,"country":32,"countryCode":20,"cosmosGeoPoint":43,"geoPoint":45,"contacts":46},"06300",{"type":34,"coordinates":44},[36,37],{"lat":37,"lon":36},[47],{"name":48,"role":24,"phone":49,"phoneExt":20,"email":26},"BEYAZIT GARİP, Principal Investigator","+905309731105",{"type":51,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"PRINCIPAL_INVESTIGATOR","Beyazit Garip","Principal Investigator","100595970","molecular-signatures-of-tms-response-in-treatment-resistant-depression-100595970",false,"NCT07039370","Molecular Signatures of TMS Response in Treatment-Resistant Depression","The Relationship Between Plasma Metabolomics and Proteomics Profiling and Response to Transcranial Magnetic Stimulation Therapy in Treatment-Resistant Depression","PROMET_TMS","Inclusion Criteria:\n\n* Diagnosis of Major Depressive Disorder (MDD) according to DSM-5-TR criteria.\n* Inadequate clinical response to at least two different antidepressants and\u002For anti-obsessive agents administered at therapeutic doses and durations.\n* Clinical symptoms not better explained by metabolic or organic medical conditions.\n* No epileptic activity detected on routine electroencephalography (EEG) prior to TMS initiation.\n* Routine pre-TMS laboratory tests reveal no abnormalities that may significantly affect treatment response, including:\n* Normal thyroid hormone profile\n* No significant vitamin deficiencies\n* No markedly elevated inflammatory markers\n* No history or current evidence of hearing loss on clinical evaluation; if present, evaluation by an otolaryngologist will be obtained.\n* Age 18 years and older.\n* Ability to provide written informed consent.\n\nExclusion Criteria:\n\n* Any contraindication to TMS as identified in the standardized pre-TMS risk assessment form.\n* Presence of epileptic focus detected on pre-TMS EEG.\n* History of significant head trauma, loss of consciousness, or intracranial surgery.\n* Presence of metal implants or foreign bodies incompatible with TMS (e.g., aneurysm clips, surgical clamps, metallic fragments).\n* Abnormal thyroid hormone levels in pre-TMS laboratory testing.\n* Significantly elevated inflammation markers (e.g., CRP) in pre-TMS bloodwork.\n* Vitamin deficiencies associated with cognitive impairment (e.g., B12, folate) in pre-TMS labs.\n* Electrolyte imbalances on pre-TMS blood testing.\n* History of psychotic disorder or bipolar I\u002FII disorder.\n* History of substance-induced psychosis or bipolar disorder.\n* Current or past substance use disorder (including alcohol, stimulants, or illicit drugs), unless abstinent from substances (excluding alcohol) for a minimum of 12 months.\n* Voluntary discontinuation of TMS during the treatment course.\n* Any serious adverse event or unexpected clinical condition during treatment that necessitates discontinuation of TMS.",true,"ALL","18 Years","65 Years",{"count":67,"type":68},55,"ESTIMATED","INTERVENTIONAL",[71],"NA","Transcranial Magnetic Stimulation (TMS) therapy is an approved and effective treatment option for treatment-resistant depression (TRD). This study aims to identify biomarkers that predict TMS treatment response in TRD, provide insights into the neurobiological mechanisms underlying TMS efficacy, and contribute to personalized treatment strategies. By establishing proteomic and metabolomic signatures, this research seeks to enhance clinical decision-making, reduce healthcare costs, and improve patient outcomes in TRD. The findings will align with the precision medicine movement in psychiatry, advancing biomarker-driven therapeutic approaches for treatment-resistant depression.",[74],"Major Depression Disorder",[17,76,77,78,79],"Metabolomics","Proteomics","Treatment Resistance","Molecular Signuture","2025-06-17",{"date":82,"type":83},"2025-06-26","ACTUAL",{"date":85,"type":83},"2025-06-15",{"date":87,"type":68},"2027-06-01",{"name":5,"class":6},2]