Skip to main content
Clinical Trials/NCT02539329
NCT02539329
Completed
Not Applicable

Characterization of Sensory Neuropathies Associated With Anti-FGFR3 Antibodies

Centre Hospitalier Universitaire de Saint Etienne17 sites in 1 country251 target enrollmentFebruary 3, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sensory Peripheral Neuropathy
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Enrollment
251
Locations
17
Primary Endpoint
Evolution of clinical and electrophysiological pattern of the neuropathy for patients with anti-FGFR3 antibodies (composite measure),
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Sensory neuronopathies affect sensory neuron in the posterior spinal ganglion. They are responsible for pain, balance disorder (ataxia) and the use of hands. They depend on multiple etiologies. In a retrospective study, the investigators showed that the anti-FGFR3 antibody is a diagnostic marker of a subset of sensory neuronopathies. The investigators believe that other antibodies can be discovered in patients who remain seronegative changing.

However, the study is retrospective and only a small number of patients could be identified. Several points therefore need to be clarified or confirmed in a second prospective study.

Detailed Description

In and out patients evaluated for a sensory neuropathy meeting the inclusion and non-inclusion criteria will be proposed to enter the study At inclusion the SSN diagnostic score is calculated and a blood sample is tested for anti-FGFR3 antibody. Follow up: Patients positive for anti-FGFR3 antibodies will be followed and evaluated clinically and electrophysiologically at 1, 6 and 12 months. A blood sample is taken at 6 and 12 months. A subgroup of patients negative for anti-FGFR3 antibodies will be randomly selected for evaluation at 1, 6 and 12 months.

Registry
clinicaltrials.gov
Start Date
February 3, 2015
End Date
January 17, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • A :Patients Male or female patient aged 18 years or more
  • Patients with a clinically pure sensory peripheral neuropathy including :
  • idiopathic or dysimmune sensory neuronopathies
  • idiopathic or dysimmune distal axonal sensory neuropathy
  • sensory chronic inflammatory demyelinating polyradiculoneuropathy
  • idiopathic or dysimmune small fiber neuropathies
  • idiopathic or dysimmune trigeminal nerve neuropathy
  • positive to antibodies anti-FGFR3
  • B :Controls Male or female patient aged 18 years or more
  • Patients with a clinically pure sensory peripheral neuropathy including :

Exclusion Criteria

  • -Motor or sensory-motor neuropathies
  • Genetic, toxic, paraneoplasic neuropathies
  • Diabetic Neuropathy.
  • Neuropathy with Anti-MAG or anti-ganglioside IgM.
  • Pregnant or breastfeeding woman

Outcomes

Primary Outcomes

Evolution of clinical and electrophysiological pattern of the neuropathy for patients with anti-FGFR3 antibodies (composite measure),

Time Frame: 6 months

Score to the Overall Disability Scale Score (ODSS), the Rankin Score, the International PrognosticScore (ISS).

Secondary Outcomes

  • Evolution of clinical and electrophysiological pattern of the neuropathy for patients with anti-FGFR3 antibodies (composite measure),(12 months)
  • Description for patients with anti-FGFR3 antibodies of the immune context(12 months)
  • Patient evolution during one year for patients with anti-FGFR3 antibodies to a control group of sensory neuropathy without antibodies(12 months)

Study Sites (17)

Loading locations...

Similar Trials