Efficacy of Non-invasive NESA Neuromodulation in Fibromyalgia
CompletedNot applicableNCT05648695
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Fibromyalgia is a chronic condition that causes pain throughout the body, fatigue and other symptoms. Among the most common clinical symptoms are sleep and anxiety disorders. All these symptoms are very disabling and have a negative impact on the quality of life of these people. There is currently no curative treatment for this pathology and current treatments focus their efforts on reducing the intensity of the symptoms. The current approach is mainly pharmacological, with the possible side effects that this entails.
Study details
- Official title
- Efficacy of Non-invasive NESA Neuromodulation in Fibromyalgia: a Randomised, Triple-blind Clinical Trial
- Conditions
- Interventions
- Device: Non-invasive Neuromodulation
- Device: Placebo Non-invasive Neuromodulation
- Sponsor
- University of Las Palmas de Gran Canaria
- Collaborators
- University of Castilla-La Mancha
- Start date
- 2022-11-01
- Primary completion
- 2023-04-01
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Spain
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients over 18 years of age * Diagnosis of Fibromyalgia meeting ACR 1990/20101,2 criteria, made by a physician, documented by a clinical report. * Diagnosis of Fibromyalgia made at least 12 months ago * Stable baseline treatment in the month prior to inclusion in the study * Signed informed consent * In normal condition and mentally competent to participate in the study. * Able to complete the study questionnaires. Exclusion Criteria: * Have any of the following contraindications for treatment with NESA XSIGNAL®: pacemakers, internal bleeding, not applying electrodes to skin in poor condition, with ulcerations or wounds, acute febrile processes, acute thrombophlebitis and/or phobia of electricity. * Failure to sign the informed consent form. * Active chronic inflammatory joint diseases. * Active neurological diseases with central or peripheral nervous system involvement. * Active systemic autoimmune diseases * Psychotic disorders * Active concomitant neoplastic or infectious processes * Medication changes in the month prior to study inclusion or throughout the duration of the study.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05648695