Condition: 1 Hz Real rTMS to the Pre-SMA · 1 Hz Sham rTMS to the Pre-SMA · Sponsor: Amsterdam UMC, location VUmc
TETRO is a multi-center placebo-controlled double-blind randomized controlled trial with an intervention phase of 5-7 weeks and a follow-up phase of 12 months in 250 adult (18 years and older) OCD patients who show no/insufficient response to ERP, aiming to establish the cost-effectiveness of low frequency (1 Hz) rTMS to the pre-SMA (compared to sham rTMS to the pre-SMA) as adjuvant treatment to exposure with response prevention (ERP). The treatment consists of 4 times/week rTMS combined with ERP for at least 5 weeks (20 sessions), with optional extension phase of 1 or 2 weeks (maximum of 28 sessions in total).
This description comes directly from the study's public registry record.
Odile A van den Heuvel, MD PhD · +31-20-4444444 · oa.vandenheuvel@amsterdamumc.nl
Tjardo S Postma, MD · +31-20-4444444 · tetro@amsterdamumc.nl
Always discuss trial participation with your own doctor first.
| Amsterdam UMC, location VU Medical Center | Amsterdam, North Holland, Netherlands | Recruiting |
| GGZ inGeest | Amsterdam, Netherlands | Recruiting |
| Neurocare | Eindhoven, Netherlands | Not Yet Recruiting |
| Neurocare | Groningen, Netherlands | Not Yet Recruiting |
| Maastricht UMC+ | Maastricht, Netherlands | Not Yet Recruiting |
| Mondriaan | Maastricht, Netherlands | Not Yet Recruiting |
| ProPersona | Nijmegen, Netherlands | Not Yet Recruiting |
| Radboudumc | Nijmegen, Netherlands | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT05331937