Subcutaneous Peripheral Nerve Stimulation (PNS) as "Hybrid Stimulation" After Failure of Spinal Cord Stimulation (SCS) to Control the Back Pain Component in Failed Back Surgery Syndrome (FBSS) Patients.(CUMPNS Study)

NCT02110888 | Completed

• 1 other identifier: CUMPNS
• Study Type: interventional
• Target: 14
• Locations: 1 country
• Sites: 1

Brief Summary

Despite globally favourable outcomes of Spinal Cord Stimulation (SCS), a significant proportion of Failed Back Surgery Syndrome (FBSS) patients do not obtain adequate coverage of low back pain. Peripheral Nerve Stimulation (PNS) has obtained the European Conformity mark for the treatment of chronic refractory neuropathic pain and is now commonly used in some countries to target back pain. However, the potential value of combining SCS and PNS as "hybrid stimulation" remains poorly described with only isolated case reports or limited experience in various indications. The "CUMPNS" comparative randomized study is designed to demonstrate the potential analgesic efficacy of PNS in addition to previously implanted SCS, to treat the residual low back pain component pain in refractory FBSS patients.

Conditions

Failed Back Surgery Syndrome

Outcome Measures

Primary Outcomes (1)

• Relative change of low back pain surface (expressed as a percentage, %)

  3 month follow-up

Study Arms (2)

SCS + PNS

EXPERIMENTAL

Mutlticolumn SCS lead + Monocolumn SCS lead

Device: Subcutaneous peripheral nerve stimulation

SCS

ACTIVE COMPARATOR

Mutlticolumn SCS lead

Other: SCS Only

Interventions

Subcutaneous peripheral nerve stimulation DEVICE

SCS + PNS

SCS Only OTHER

SCS

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age ≥ 18 years and ≤ 80 years.
• History of FBSS after one or more surgical procedures on the spine, treated with SCS,
• Failure of well conducted conservative treatment (drug or non-drug).
• Patients implanted with a single-column or multicolumn SCS lead providing significant relief of the radicular pain component.
• Persistent failure on the low back pain component despite the efficacy of SCS on the radicular pain component.
• Patients with documented residual neuropathic low back pain (DN4, sensorimotor studies, clinical examination, pain characteristics, etc.).
• Patients with significant residual low back pain with mean intensity on Visual Analogue Scale (VAS) ≥ 40 mm) despite Conventional Medical Management (CMM) and SCS (mean measure calculated on daily VAS scores on 5 consecutive days).
• Positive response to Transcutaneous Electrical Nerve Stimulation (TENS) trial on the back pain component.
• Patients understanding and accepting the study constraints.
• Patients covered by French national health insurance.
• Patients have signed the Informed Consent Form after being provided with clear and honest information about the study.
• Absence of active psychosis or serious psychotic history requiring hospitalisation.
• Absence of active cancer.

You may not qualify if:

• Age \< 18 years and \> 80 years.
• Back pain amenable to further aetiological biomechanical surgery (discogenic pain, spinal instability, spinal deformity, etc.).
• Surgical, psychiatric or anaesthetic contraindication to PNS lead implantation.
• Negative response to TENS trial.
• Absence of signature of the informed consent form.
• Patients not covered by French national health insurance.
• Subjects requiring closer protection, i.e. minors, pregnant women, nursing mothers, subjects deprived of their freedom by a court or administrative decision, subjects admitted to a health or social welfare establishment, major subjects under legal protection, and finally patients member of a high-risk population.
• Women of childbearing age not using effective contraception.

Sponsors & Collaborators

• Poitiers University Hospital: lead

Study Sites (1)

Poitiers University Hospital

Poitiers, 86021, France

Location

MeSH Terms

Conditions

Failed Back Surgery Syndrome

Condition Hierarchy (Ancestors)

Postoperative Complications; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Back Pain; Pain; Neurologic Manifestations; Signs and Symptoms

Study Officials

• Philippe RIGOARD, MD, PhD

  Poitiers University Hospital

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 4, 2014
• First Posted: April 10, 2014
• Study Start: February 1, 2013
• Primary Completion: October 14, 2018
• Study Completion: October 14, 2018
• Last Updated: October 18, 2021

Record last verified: 2021-09

Locations

FR (1)