Dorsal Root Ganglion Stimulation for the Management of Painful Intractable Small Fibre Neuropathy: (NSI-TD-002)

Lugano Regional Hospital

Status: Unknown

Conditions: Neuropathy Small Fibre

Treatments: Device: Spinal Modulation Axium™

Study type: Interventional

Funder types: Other

Identifiers

NCT02435004

NSI-TD-002

Details and patient eligibility

About

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).

Full 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).

Enrollment: 31 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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31 participants in 1 patient group

Spinal Modulation Axium™

Other group

Description:

Spinal Modulation Axium™: an external trial neurostimulator (TNS) is used for the trial period, followed by an implanted neurostimulator (INS) if the TNS is successful. The TNS and INS are a pacemaker-sized devices that send out mild electrical pulses. The stimulator contains a battery and electrical components. Both TNS and INS are constant voltage devices. The TNS is used first and is worn on the outside of the clothing. The INS is implanted under the skin and support:

Treatment:

Device: Spinal Modulation Axium™