Skip to content
Trial Eligibility
Menu

Spatiotemporal Thalamocortical Alterations Underlie Experimental and Chronic Pain

NCT06968689

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this study is to assess thalamocortical (TC) connectivity during tonic pressure pain, to evaluate alpha activity during tonic pressure pain and to determine pressure pain ratings by using Electroencephalography (EEG), Functional Magnetic Resonance Imaging (fMRI), Transcranial Alternating Current Stimulation (tACS), sham and Transcranial random noise stimulation (tRNS)

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Pain

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
18 to 60 years
Sex
All
Healthy volunteers
Accepted
Sponsor
The University of Texas Health Science Center, Houston
Last updated on ClinicalTrials.gov
March 2, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Texas · 1

  • The University of Texas Health Science Center at Houston · Houston, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.