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Recruiting NCT06490965

NCT06490965 Improving Obsessive-compulsive Disorder Treatments: from Lesions to Neuromodulation Targets

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Clinical Trial Summary
NCT ID NCT06490965
Status Recruiting
Phase
Sponsor Fundacao Champalimaud
Condition Obsessive-Compulsive Disorder
Study Type INTERVENTIONAL
Enrollment 32 participants
Start Date 2024-11-07
Primary Completion 2026-12-31

Trial Parameters

Condition Obsessive-Compulsive Disorder
Sponsor Fundacao Champalimaud
Study Type INTERVENTIONAL
Phase N/A
Enrollment 32
Sex ALL
Min Age 18 Years
Max Age 75 Years
Start Date 2024-11-07
Completion 2026-12-31
Interventions
Repetitive Transcranial Magnetic StimulationNeuronavigationMagnetic Resonance Imaging

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Brief Summary

While in most cases of obsessive-compulsive disorder (OCD) a cause cannot be identified, this syndrome may develop as a consequence of focal brain lesions. Neuropsychiatric disorders secondary to brain insults are open windows to understand their underlying neurobiology. Different neuroimaging analysis methods, including pooled lesion topography and lesion network mapping, can be used to study lesional neuropsychiatric syndromes, including OCD. If successful, these strategies can also reveal new neuromodulation treatment targets, including for transcranial magnetic stimulation (TMS). Indeed, TMS targets to treat depression evolved from evidence extracted from lesional studies that were then refined and validated. For OCD treatment with TMS, already approved by the FDA and European Commission, targets were defined using a distinct approach, not involving causal brain lesions, which may contribute to lower than desirable remission rates. Lesional OCD is characterized by specific dysfunctional brain circuits. These circuits may be effectively targeted by TMS, which may optimize treatment of OCD. To address these hypotheses, we will test the therapeutic benefits of optimizing brain targets for the currently used TMS treatment of OCD, using information from the lesional-OCD brain network namely refining the target in the medial orbitofrontal cortex, bilaterally. Specifically, we will conduct a randomized clinical interventional study, using TMS to treat patients with OCD with inadequate response to other treatments, comparing, within the approved protocol for OCD treatment, the most frequently used stimulation site with a new target, adjusted according to the connectivity of lesions associated with the occurrence of OCD. If successful, our results may have immediate clinical implications in OCD treatment, as it will contribute to refine current therapeutic TMS strategies for OCD and defining new clinical research strategies in this domain.

Eligibility Criteria

Inclusion Criteria: * Age between 18 and 75 years; * Established diagnosis of Obsessive-Compulsive Disorder according to Diagnostic and statistical manual of mental disorders 5 (DSM5) criteria; * Capacity to give consent; * Fluent in Portuguese and/or English; * If potential for pregnancy, agrees to use an effective method of contraception throughout the study period. Exclusion Criteria: * Obsessive-compulsive symptoms severity assessed at baseline visit with the instrument Yale-Brown Obsessive Compulsive Scale - II (YBOCS-II) ≤ 24; * Presence of uncontrolled active medical illness; * Known structural lesion of the central nervous system; * Electric or metallic implants in the body not compatible with electromagnetic radiation; * Electric or metallic brain implants; * Cardiac implants; * Epilepsy; * Pregnant, breastfeeding, or planning pregnancy women; * Alcohol or substance abuse and/or dependence; * Major Neurocognitive Disorder; * Developmental disorders with low intelligence quotie

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