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Transcranial Magnetic Stimulation
Transcranial magnetic stimulation (TMS) for Chemobrain
N/A
Waitlist Available
Led By Phillip Kuo, MD
Research Sponsored by University of Arizona
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 days
Awards & highlights
Study Summary
This trial will test if a treatment called rTMS can help people with PCCI. The study will use tests to measure how well the treatment works.
Eligible Conditions
- Chemobrain
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ two weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~two weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Memory Testing
Secondary outcome measures
Test for improved brain functional connectivity on fMRI.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Transcranial magnetic stimulation (TMS)Experimental Treatment1 Intervention
We propose to test the efficacy of rTMS for the treatment of PCCI. Efficacy measures will include baseline and post-rTMS neuropsychological testing, functional MRI and biometry data using body worn sensors.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Transcranial magnetic stimulation (TMS)
2013
Completed Phase 4
~510
Find a Location
Who is running the clinical trial?
University of ArizonaLead Sponsor
514 Previous Clinical Trials
148,593 Total Patients Enrolled
Phillip Kuo, MDPrincipal InvestigatorUniversity of Arizona
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