Dorsal Root Ganglion Stimulation for the Management of Painful Intractable Small Fibre Neuropathy:

Not Applicable

• Conditions: Neuropathy Small Fibre

• Registration Number: NCT02435004
• Lead Sponsor: Ospedale Regionale di Lugano

Brief Summary

A prospective, single-arm, mono-centre pilot study to obtain preliminary information on the ability of Dorsal Root Ganglion Stimulation (DRGS) in alleviating the painful symptoms in patients with small fiber neuropathy (SFN).

Detailed Description

This study is a prospective, single-arm, mono-centre pilot study enrolling a maximum of 31 patients with SFN. All enrolled patients will receive a trial neurostimulation (TNS) lasting from 3 to 30 days and only patients with a positive result in terms of pain intensity reduction will be eligible for the implanted neurostimulation (INS) phase. The target number of patients eligible for INS is 10 and this population will be assessed for impact of DRGS on the neuropathic pain caused by SFN. The expected duration of patients participation will be 14 months. The rationale for this open label approach is that this is a novel technique for which pilot data with regard to applicability and efficacy have yet to be established. Data gathered in the study will provide preliminary data required to assess the feasibility of this intervention, to be used for possible future studies with a more rigorous methodological approach (i.e. controlled trial, randomized controlled trial).

Study Timeline

• Study Start: 2015-04
• Study First Submitted: 2015-04-15
• Study First Submitted QC: 2015-04-30
• Study First Posted: 2015-05-06
• Status Verified: 2021-03
• Last Update Submitted: 2021-03-24
• Last Update Posted: 2021-03-26
• Primary Completion: 2022-04
• Study Completion: 2023-04

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 31

Inclusion Criteria

• 18 years or older at inclusion
• Chronic, intractable painful SFN in the peripheral limbs during at least 12 months and a biopsy positive for SFN, with a chronic pain intensity of ≥ 6 on a Numeric Rating Scale (ranging from 0 to 10), for which previous drug therapy was unsuccessful
• Stable medication dosage in the 30 days prior to inclusion
• Stable pattern of neurological symptoms

Exclusion Criteria

• Known or suspected non-compliance
• Drug or alcohol abuse
• Pain predominantly in upper limbs
• Neuropathy or chronic pain in limbs of other origin than SFN
• Peripheral vascular disease
• Severe foraminal stenosis at the expected target level
• Coagulation disorders
• Known immune-deficiency
• Other significant concomitant diseases and any concomitant malignancies
• Presence of other indwelling devices

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Change in pain intensity assessed by Numeric Rating Scale.	Pain intensity assessment during 2 weeks after inmplatation, at Time point 6 and 12 months after implantation.	Four assessments/day for 5 consecutive days around the intended measurement timepoint

Trial Locations

Locations (1)

EOC Lugano; 🇨🇭 Lugano, Ticino, Switzerland