Sign and Symptoms: Pain Signs and Symptoms Pain
Conditions
Interventions
15 volunteers will complete an fMRI scanning protocol on 4 separate study days on each of which they will receive one of 3 CMEs or a placebo treatment. During the scanning protocol, volunteers will re
Sponsors
Department of Health
Eligibility
Inclusion criteria
Inclusion criteria: Not provided at time of registration
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Volunteers' rating of pain during noxious thermal stimulation 2. BOLD response associated with thermal stimulation after the 3 CMEs treatments and the placebo treatment sessions. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed