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Fibromyalgia and Small Fiber Neuropathy

Recruiting
Conditions
Chronic Pain Syndrome
Interventions
Diagnostic Test: Skin punch biopsy to demonstrate small fiber neuropathy
Registration Number
NCT06527183
Lead Sponsor
Hospital Ambroise Paré Paris
Brief Summary

The primary objective of this study will be to assess the proportion of fibromyalgia patients with diffuse small-fiber neuropathy (i.e. in the upper and lower limbs) and compare this proportion to patients with other chronic pains (nociplastic, nociceptive) and with healthy controls. Our analysis will be based on the demonstration of structural abnormalities of small nerve fibers by means of skin biopsy, but also of functional abnormalities using four validated tests commonly used in this field: quantitative sensory testing (QST), laser evoked potential recordings, Sudoscan and confocal corneal microscopy. It will thus be possible to verify whether or not patients with small fiber neuropathy have a particular clinical profile in terms of pain, physical activity, comorbidities or pain impact.

Detailed Description

Small fiber neuropathy has been observed in a large proportion of fibromyalgia patients. However, the pathophysiological role of these neurological abnormalities in determining the pain and other symptoms of fibromyalgia, and the specificity of these abnormalities, are not well understood.

The primary objective of this study will be to assess the proportion of fibromyalgia patients with diffuse small-fiber neuropathy (i.e. in the upper and lower limbs) and compare this proportion to patients with other chronic pains (nociplastic, nociceptive) and with healthy controls. Our analysis will be based on the demonstration of structural abnormalities of small nerve fibers by means of skin biopsy, but also of functional abnormalities using four validated tests commonly used in this field: quantitative sensory testing (QST), laser evoked potential recordings, Sudoscan and confocal corneal microscopy. It will thus be possible to verify whether or not patients with small fiber neuropathy have a particular clinical profile in terms of pain, physical activity, comorbidities or pain impact.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • patients over 18 years of age with no age limit -
  • having given their signed consent to take part in the study
  • affiliated to the French social security system
  • able to be followed for the entire duration of the study
  • reading and understanding French
  • accepting the principle of the study and able to comply with its conditions
  • suffering from chronic pain for at least six months of at least moderate intensity (≥ 4/10)
  • fibromyalgia detected by the FiRST questionnare and defined by the revised diagnostic criteria of the WHO or chronic nociceptive or nociplastic pain without associated fibromyalgia.
  • chronic pain for at least 6 months of at least moderate intensity (≥ 4/10)
  • untreated or with stable analgesic treatment for at least 2 weeks prior to inclusion- normal neurological examination at inclusion
Exclusion Criteria
  • litigation or compensation-seeking
  • cancer for less than 2 years
  • known cause of small-fiber neuropathy such as diabetes, systemic disease, hypothyroidism, alcohol, renal failure, genetic disease
  • clinical or EMG neuropathy
  • peripheral or central nervous system pathology with or without associated neuropathic pain
  • uncontrolled chronic pathology such as : morbid obesity, sleep apnea, uncontrolled hypertension, etc. - psychosis, previous suicide attempt
  • drug or psychoactive substance abuse
  • cognitive or psychological disorders incompatible with compliance with and/or understanding of the protocol
  • participation in another biomedical research protocol.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Patients with fibromyalgiaSkin punch biopsy to demonstrate small fiber neuropathyPatients with fibromyalgia based on ACR criteria
Patients with other chronic pain (paired for the other groups)Skin punch biopsy to demonstrate small fiber neuropathyPatients with chronic pain other than fibromyalgia and neuropathic pain, eg nociplastic pains or nociceptive pains
Paired healthy subjectsSkin punch biopsy to demonstrate small fiber neuropathyHealthy subjects paired for gender and age
Primary Outcome Measures
NameTimeMethod
Prevalence of small fiber neuropathy or pathology as assessed with skin punch biopsy in patients with fibromyalgia as compared to patients with other chronic pains and healthy subjectsBaseline and at 6 months

intraepidermal nerve fiber density

Secondary Outcome Measures
NameTimeMethod
Monitor the evolution of abnormalities obtained over time (6 months) and correlate them with the evolution of pain and associated symptoms.6 months

Comparison of intraepidermal nerve fiber density and other diagnostic measures between baseline and 6 months

Correlation between intraepidermal nerve fiber density and pain or other patient reported outcome measures (quality of life, distress, disability...)Baseline and at 6 months

Correlation statistics (Spearman Rho)

Determine the sensitivity and diagnostic value of corneal confocal microscopy and laser evoked potentials as compared with skin punch biopsy for exploring nociceptive fibersBaseline and at 6 months

Sensitivity and specificy of these tests compared to skin punch biopsy

Determine the diagnostic value of the sudoscan and quantified sensory tests compared with other tests for exploring nociceptive fibers in these patientsBaseline and at 6 months

Sensitivity and specificy of sudoscan and quantitative sensory testing compared to skin punch biopsy

Investigate the potential specificity of the results obtained by comparing them with pain patients without fibromyalgia or nerve damage (patients with any nociceptive or nociplastic pain without fibromyalgia) matched for age and genderBaseline and at 6 months

Direct group comparisons

Trial Locations

Locations (2)

Inserm U987

🇫🇷

Boulogne-Billancourt, France

Centre d'Evaluation et de Traitement de la douleur

🇫🇷

Paris, France

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