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Trials. 2020 Jan 28;21(1):111. doi: 10.1186/s13063-019-3831-4.

Multicentre, double-blind, randomised, sham-controlled trial of 10 khz high-frequency spinal cord stimulation for chronic neuropathic low back pain (MODULATE-LBP): a trial protocol.

Author information

1
Pain Management & Neuromodulation Centre, St Thomas' Hospital, Westminster Bridge Road, SE1 7EH, London, UK. alkaisy@aol.com.
2
Guys & St. Thomas NHS Foundation Trust, London, UK.
3
Institute of Health and Well Being, University of Glasgow, Glasgow, UK.
4
Institute of Health Research, University of Exeter Medical School, Exeter, UK.
5
Wessex Institute, University of Southampton, Southampton, UK.
6
University Hospital Southampton NHS Foundation Trust, Southampton, UK.
7
South Tees Hospitals NHS Foundation Trust, Middlesbrough, UK.
8
Department of Psychology, Uppsala University, Uppsala, Sweden.
9
Liverpool Reviews and Implementation Group, Health Services Research, University of Liverpool, Liverpool, UK.
10
University of Oxford, Oxford, UK.

Abstract

INTRODUCTION:

Chronic neuropathic low back pain (CNLBP) is a debilitating condition in which established medical treatments seldom alleviate symptoms. Evidence demonstrates that high-frequency 10 kHz spinal cord stimulation (SCS) reduces pain and improves health-related quality of life in patients with failed back surgery syndrome (FBSS), but evidence of this effect is limited in individuals with CNLBP who have not had surgery. The aim of this multicentre randomised trial is to assess the clinical and cost-effectiveness of 10 kHz SCS for this population.

METHODS:

This is a multicentre, double-blind, randomised, sham-controlled trial with a parallel economic evaluation. A total of 96 patients with CNLBP who have not had spinal surgery will be implanted with an epidural lead and a sham lead outside the epidural space without a screening trial. Patients will be randomised 1:1 to 10 kHz SCS plus usual care (intervention group) or to sham 10 kHz SCS plus usual care (control group) after receiving the full implant. The SCS devices will be programmed identically using a cathodal cascade. Participants will use their handheld programmer to alter the intensity of the stimulation as per routine practice. The primary outcome will be a 7-day daily pain diary. Secondary outcomes include the Oswestry Disability Index, complications, EQ-5D-5 L, and health and social care costs. Outcomes will be assessed at baseline (pre-randomisation) and at 1 month, 3 months and 6 months after device activation. The primary analyses will compare primary and secondary outcomes between groups at 6 months, while adjusting for baseline outcome scores. Incremental cost per quality-adjusted life year (QALY) will be calculated at 6 months and over the lifetime of the patient.

DISCUSSION:

The outcomes of this trial will inform clinical practice and healthcare policy on the role of high-frequency 10 kHz SCS for use in patients with CNLBP who have not had surgery.

TRIAL REGISTRATION:

Clinicaltrials.gov, NCT03470766. Registered on 20 March 2018.

DISCLAIMER:

The views expressed here are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health. The NIHR had no role in the study design, writing of the manuscript or the decision to submit for publication.

ROLES AND RESPONSIBILITIES:

AK, SP, DP, SW, RST, AC, SE, LM, RD and JF all contributed to the trial design and to securing trial funding. AK, JR, SP, DP, and SE are involved in the recruitment, the intervention and the follow-up. SW will perform data collection and analysis. RST will be responsible for the statistical analysis, and RD will be responsible for the health economic analysis. All authors read and approved the final manuscript.

KEYWORDS:

Spinal cord stimulation, Neuropathic pain, Chronic neuropathic low back pain, Neuromodulation

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