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:
- Adults aged 18 to 99 years old at the time of screening
- People who understand what the study involves, agree to its procedures, and sign a written consent form before any study activities begin
- People who have been living with chronic pain from myofascial pain syndrome (a condition involving muscle and soft tissue pain) for at least 3 months, where the pain is specifically low back pain, tension headaches, or neck pain, and where myofascial pain syndrome is the main cause of that pain
- People whose pain treatment has stayed the same for at least 1 week during the screening period
- People whose pain scores average 4 or more (on a 0–10 scale) on at least 4 out of 7 days during the screening period
- People who have shown they can consistently complete the required daily pain reporting
Who may not be able to join:
- People who have active implanted medical devices (such as a pacemaker)
- People who have an allergy to the emergency or backup medication used in the study
- People who are pregnant
- People who have mental or physical conditions that could make using the study device unsafe
- People who have epilepsy or cerebral spasms
- People who have a psychiatric illness or a pain condition classified as somatoform (where psychological factors are a primary driver)
- People who are taking high-dose opioid pain medication (equivalent to more than 120mg of oral morphine per day)
- People who are taking centrally acting muscle relaxants, such as Sirdalud (tizanidine) or benzodiazepines
- People who have a medical reason they cannot take anti-inflammatory medications (NSAIDs)
- People who have artificial joints made from methylmethacrylate or polyethylene at the area where the study device would be used
- People who have ferromagnetic metal implants (such as certain aneurysm clips or dental implants) at the area where the study device would be used
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: Rudolf Likar, Prof. Dr., Klinikum Klagenfurt am Wörthersee
Phone: +49 1511 0177825
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
Average Numeric Rating Scale (NRS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.