Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06865222

Post COVID-19 Syndrome Treatment With Variable Pulse Transcranial Magnetic Stimulation

Variable Pulse Transcranial Magnetic Stimulation for Treatment of Post COVID Syndrome

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test if Variable Pulse TMS (Transcranial Magnetic Stimulation) can result in objective improvements in patients with Post COVID Syndrome (PCS).

Conditions

Interventions

TypeNameDescription
PROCEDUREElectromagnetic Brain Pulsing Variable Pulse Protocol (EMBP) - 2 weeksThe Electromagnetic Brain Pulsing Variable Pulse Protocol (EMBP) will be administered through an FDA-approved Transcranial Magnetic Stimulation (TMS) medical device. Results of the baseline EEG will be uploaded to NoetherTech's EMBP software on the Mayo Clinic campus, and transferred to Noethertech servers for TMS parameter determination TMS treatment will be one 30 min session per day, 5 days per week (Monday-Friday), for 2 weeks.
PROCEDUREElectromagnetic Brain Pulsing Variable Pulse Protocol (EMBP) - 4 weeksThe Electromagnetic Brain Pulsing Variable Pulse Protocol (EMBP) will be administered through an FDA-approved Transcranial Magnetic Stimulation (TMS) medical device. Results of the baseline EEG will be uploaded to NoetherTech's EMBP software on the Mayo Clinic campus, and transferred to Noethertech servers for TMS parameter determination TMS treatment will be one 30 min session per day, 5 days per week (Monday-Friday), for 4 weeks.

Timeline

Start date
2025-07-22
Primary completion
2027-01-01
Completion
2027-04-01
First posted
2025-03-07
Last updated
2025-08-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06865222. Inclusion in this directory is not an endorsement.