Fibromyalgia Trial, Recruiting NCT07494162 Sponsor: University of California, Davis Condition: Fibromyalgia
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Fibromyalgia Trial, Recruiting

NCT07494162
Recruiting Not Applicable

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:

  • You are able to understand what the trial involves and are willing to sign a consent form agreeing to take part
  • You are willing and able to follow all the steps and procedures required by the trial
  • You are willing to be randomly assigned to receive either real acupuncture or fake (sham) acupuncture
  • You currently have chronic low back pain that has lasted at least 3 months AND has caused pain on more than half of the days over the past 6 months
  • You have at least one tight knot or firm band of muscle that can be felt by touch in the muscles of your lower back, side, or buttocks
  • When a doctor presses on one of those tight muscle knots or bands, it brings on the main pain you have been experiencing
  • Your main pain is felt near the centre of your back, either on one side or both sides
  • You are willing and able to lie still on your back for a brain/body scan (called a TB-PET/CT scan) lasting about 70 minutes, at least twice and ideally three times
  • You are willing and able to avoid eating or drinking (fast) for at least 6 hours before each scan and throughout the scan
  • You are willing to avoid hard physical exercise for 24 hours before each scan visit
  • You are willing to use effective birth control methods throughout the study

Who may not be able to join:

  • You do not have a Primary Care Physician (family doctor)
  • You have a history of infection in your spine or a tumour affecting your spine
  • You have been diagnosed with ankylosing spondylitis, rheumatoid arthritis, polymyalgia rheumatica, psoriatic arthritis, or lupus
  • You have another condition that is known to be causing your pain
  • You have any implants in or near the area of the body being studied
  • You have been diagnosed with a broken vertebra (spinal bone) in the last 6 months
  • You have a condition affecting the nerves at the base of your spine that causes significant weakness in your legs (confirm with trial site)
  • You have any spinal implants — such as metal rods, screws, a spinal cord stimulator, or a drug pump — in the area being studied
  • Your pain mainly comes from the nervous system itself rather than from a specific body part (confirm with trial site)
  • You have pain that goes below your knee
  • You have a positive result on a specific physical test for nerve problems in the leg called the straight leg raise test
  • You have hip joint arthritis that is causing symptoms
  • You have severe claustrophobia that is not under control
  • You are currently pregnant or breastfeeding
  • You weigh more than 225 kg (496 pounds), due to the weight limit of the scanning equipment
  • You are currently in prison
  • You are unable to speak, read, and write in English
  • You have had a PET scan as part of another research study within the last 12 months (this does not include PET scans done as part of your regular medical care)
  • The lead researcher decides there is any other reason that taking part would not be appropriate for you

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Abhijit J Chaudhari, PhD, University of California, Davis

Phone: 916-731-9004

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

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
18 May 2026
Est. completion
1 April 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in PEG score from Baseline to 8 weeks; Change in Standardized Uptake Values in Myofascial Regions of Interest on TB-PET/CT from Baseline to 8 weeks

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov