CompletedNot Applicable

Repetitive Transcranial Magnetic Stimulation in Fibromyalgia

France42 participantsStarted 2011-04

Plain-language summary

The purpose of this study is to determine the analgesic effectiveness of Repetitive Transcranial Magnetic Stimulation (rTMS) used as an additional procedure to rehabilitation exercises in patient suffering from fibromyalgia. A double blind clinical trial with two randomized parallel groups: * Placebo rTMS and rehabilitation exercise * Active rTMS and rehabilitation exercise

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * primary fibromyalgia according to the American College of Rheumatology * no contraindication to rehabilitation exercise * pain with VAS \> 4 during at least six months * FIQ score \> 50 * no change in drug therapy over the last month * affiliation to French Health Service Exclusion Criteria: * BMI \> 35kg/m² * patient who has already benefited from rTMS * rTMS contraindication * restless legs symptom * patient suffering from major depression * patient suffering from inflammatory rheumatism, autoimmune disease, other chronic pain pathology * sleep apnea syndrome * no contraindication to rTMS or MRI * pregnant women

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Change from baseline in pain Visual Analog Scale (VAS) at 14 weeks of treatment

Timeframe: Daily average VAS at baseline, week 2, week 4, week 8, week 14

Trial details

NCT IDNCT01308801

SponsorUniversity Hospital, Grenoble

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-09

View on ClinicalTrials.gov More Fibromyalgia trials