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izvor podataka: crosbi

Efficacy and safety of repetitive transcranial magnetic stimulation using an H1-coil or figure-8- coil in the treatment of unipolar major depressive disorder : a study protocol for a randomized controlled trial (CROSBI ID 259563)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Filipčić, Igor ; Šimunovic Filipčić, Ivona ; Gajšak, Tomislav ; Milovac, Željko ; Sučić, Strahimir ; Ivezić, Ena ; Zečević Penić, Sandra ; Orgulan, Ivana ; Šebo, Damir ; Jeleč, Vjekoslav et al. Efficacy and safety of repetitive transcranial magnetic stimulation using an H1-coil or figure-8- coil in the treatment of unipolar major depressive disorder : a study protocol for a randomized controlled trial // Psychiatria Danubina, 30 (2018), 1; 41-46. doi: 10.24869/psyd.2018.41

Podaci o odgovornosti

Filipčić, Igor ; Šimunovic Filipčić, Ivona ; Gajšak, Tomislav ; Milovac, Željko ; Sučić, Strahimir ; Ivezić, Ena ; Zečević Penić, Sandra ; Orgulan, Ivana ; Šebo, Damir ; Jeleč, Vjekoslav ; Bajić, Žarko

engleski

Efficacy and safety of repetitive transcranial magnetic stimulation using an H1-coil or figure-8- coil in the treatment of unipolar major depressive disorder : a study protocol for a randomized controlled trial

Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive technique with few side effects that has been reported to be effective in the treatment of major depressive disorder (MDD). At present, no randomized controlled trials (RCT) have compared the efficacy and safety of rTMS delivered by the figure-8-coil and the H1-coil. We describe an industry-independent, randomized, controlled, single-blinded, single-center study protocol assessing the differences in efficacy and safety of rTMS for patients diagnosed with MDD with the H1-coil and figure-8-coil as an add-on to stable pharmacotherapy or pharmacotherapy alone. Stimulation protocols follow those that led to the FDA clearance of these treatments for MDD. The sample of 76 patents in each of the three groups will be enrolled and assessed with clinical and neuropsychological tests. The primary outcome is remission rate defined as Hamilton depression rating scale (HAM-D17) score <= 7 at the end of week-4. This clinical trial will address the efficacy and safety of rTMS modalities for MDD. The evaluation of biological markers will also help to elucidate the pathophysiology of MDD and the mechanisms of action of rTMS.

repetitive transcranial magnetic stimulation rTMS ; deep TMS dTMS ; major depressive disorder

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Podaci o izdanju

30 (1)

2018.

41-46

objavljeno

0353-5053

1849-0867

10.24869/psyd.2018.41

Povezanost rada

Kliničke medicinske znanosti

Poveznice
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