Fibromyalgia Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are between 18 and 80 years old
- People who have been diagnosed with Fibromyalgia for more than 6 months
- People who are already taking opioid pain medication every day on an ongoing basis, such as Hydrocodone (Norco), Oxycodone (Percocet), morphine, methadone, or Tylenol #3
- People whose pain is rated at 5 or higher out of 10 on a standard pain scale at the start of the trial
Who may not be able to join:
- People who are younger than 18 or older than 80 years old
- People who have been diagnosed with a Substance Use Disorder (SUD)
- People who are pregnant
- People who have an active legal case related to an injury, such as a lawsuit or worker's compensation claim
- People who have an active mental health diagnosis such as bipolar disorder, psychosis, or thoughts of suicide
- People who are currently prescribed and taking low-dose Naltrexone
- People who have had acupuncture treatment within the last 6 months
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Ariana Nelson, MD, University of California, Irvine
Phone: 6262550574
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in the pain VAS versus time following opioid challenge for pre-post TA vs. pre-post SA
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.