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The purpose of this study is to perform an open label feasibility trial of TMS for the treatment of chronic scrotal content pain.
Full description
The purpose of this study is to perform an open label feasibility trial of TMS for the treatment of chronic scrotal content pain. Participants will be screened by study staff for contraindications to TMS treatment. TMS will be delivered use the MagVenture TMS machine. TMS will be delivered during 15 minutes per session, 3 sessions each day, for 3 days. A custom developed SMS text EMA system will be used to gather daily data on pain and functioning in study participants.
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Interventional model
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50 participants in 1 patient group
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Central trial contact
Solomon Hayon, MD
Data sourced from clinicaltrials.gov
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