Optimizing Accelerated TMS for Chronic Pain With Thompson Sampling
- NCT ID
- NCT07103135
- Registry status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 1
- Sponsor
- University of Minnesota
- Conditions
- Chronic Pain
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 30 participants (Estimated).
What is being studied
- Device: MagVenture X100 Pro transcranial magnetic stimulation system
Who may be eligible
- Ages
- 18 Years to no maximum
- Sex
- All
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* Ages 18 years or older
* Ability to provide written informed consent
* Ability to read and to communicate verbally and in writing in English
* Chronic pain persisting for at least 12 months
* Pain refractory to oral pain medication (defined as failing at least two different medication classes)
* Average pain intensity of ≥5 on the Numerical Rating Scale (NRS) over the past two weeks
* Stable pain medication regimen for at least 4 weeks prior to enrollment
* Willing and able to attend all study visits and comply with study procedures
Exclusion Criteria:
* Current substance use disorder (except for nicotine or cannabis) as determined by DSM-5 criteria
* Active suicidal ideation with intent or plan as determined by the Columbia-Suicide Severity Rating Scale (C-SSRS)
* Lifetime history of bipolar disorder, schizophrenia, or other psychotic disorder as determined by medical history
* Self-reported unstable medical conditions that would pose increased risks for TMS or MRI
* Pregnancy (as determined by urine pregnancy test) or planned pregnancy during the study period
* Contraindications to TMS, including:
* History of seizure or epilepsy
* Metallic implants in the head (excluding dental fillings)
* Cardiac pacemaker or other implanted medical devices
* History of significant head trauma
* History of intracranial surgery
* Medication that significantly lowers seizure threshold that cannot be safely held
* Contraindications to MRI, including:
* Claustrophobia
* Metallic implants or devices
* Inability to lie flat for the duration of the scan
* Current use of high-dose opioids (\>90 morphine milligram equivalents daily)
* Participation in another clinical trial of an investigational medication or device within 30 days prior to enrollment
* Any condition that, in the investigator\'s opinion, would make it unsafe or difficult for the participant to complete the study
Study locations
1 study location is listed.
Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.
Countries: United States
- Minnesota, United States: 1
Sample of listed locations
- University of Minnesota — Minneapolis, Minnesota, 55455, United States — Recruiting
Study details
- Start date
- March 1, 2026
- Primary completion date
- August 31, 2030
- Completion date
- August 31, 2030
- First posted
- August 5, 2025
- Collaborators
- The Foundation for the Advancement of Clinical TMS
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07103135
- Registry last updated
- March 27, 2026
- QualifiedStudies registry data refreshed
- October 2, 2026
- QualifiedStudies record fetched
- October 2, 2026
View NCT07103135 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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