An observational study in Pain, sponsored by National Center for Complementary and Integrative Health (NCCIH). Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-12-09.
Sponsored by National Center for Complementary and Integrative Health (NCCIH) · Observational
Background:
Objectives:
Eligibility:
Design:
Different pain reducing drugs work in different ways to reduce pain. Many drugs, including morphine and codeine, reduce pain by binding to opiate receptors in the brain. Another chemical, naloxone, can block the effect of these drugs. In this study, we are looking at brain responses to a pain-relieving cream and whether naloxone blocks the effect of the cream. We will compare the results of people with chronic pain (fibromyalgia) to those of people without chronic pain.
Design:
The study compares MRI response to painful stimulation between people with fibromyalgia and healthy volunteers under two conditions: 1) naloxone, 2) placebo.
Outcome measures: Pain ratings and pain-related MRI responses are compared between people with fibromyalgia and healthy volunteers
2,928 studies on the registry are indexed under Chronic Pain; 699 are open to participants now.
This study's enrollment of 92 is below the median of 126 across 687 observational studies indexed under Chronic Pain.
Browse Chronic Pain studies →National Center for Complementary and Integrative Health (NCCIH) is the lead sponsor of 218 studies on the registry; 7 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Inclusion Criteria for Patients:
Inclusion Criteria for Healthy Controls:
EXCLUSION CRITERIA:
Exclusion criteria for patients:
Exclusion criteria for healthy controls:
Pain Perception
Time frame: 3 years
This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.
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National Center for Complementary and Integrative Health (NCCIH)