CompletedNot Applicable

Dose-Efficacy of rTMS in Healthy Young Female Volunteers

Spain10 participantsStarted 2024-01-11

Plain-language summary

This study is aimed to develop a new therapy based on non-invasive repetitive magnetic stimulation rehabilitation for FI in patients who do not respond to conventional therapies.

Who can participate

Age range18 Years – 35 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * no history of FI * Be a woman * capable of understanding and providing informed consent Exclusion Criteria: * pregnancy and the ability to become pregnant * presence of a pacemaker * history of epilepsy or neurosurgery * poor treatment tolerance

What they're measuring

MEP Latency

Timeframe: Baseline (immediately before stimulation) and immediately after stimulation in each session, across 5 weekly sessions (up to 5 weeks).

Trial details

NCT IDNCT07192328

SponsorHospital de Mataró

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-04-01

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