Study on Failed Back Surgery Syndrome Pathway Optimization: A Focus on Patient Identification, Chronicization Factors and Outcome Predictors

Not Applicable

Completed

• Conditions: Chronic Pain; Failed Back Surgery Syndrome
• Interventions: Other: No name

• Registration Number: NCT02964130
• Lead Sponsor: Poitiers University Hospital

Brief Summary

This pilot study is part of a global project that aims to better define and understand features of FBSS/POPS "post-operative persistent syndrome patients (shortened as "FBSS" in the following project). FBSS is the acronym for Failed Back Surgery Syndrome, which has been defined as a chronic condition resulting from spinal interventions. Despite anatomically successful spine surgery, a significant proportion of patients is experiencing chronic refractory back and leg pain. In a recent multicentre study conducted on more than 100 refractory FBSS patients, (ESTIMET Study), the mean delay between pain occurrence and FBSS diagnosis was 5 years. Therefore, FBSS pattern and potential responder stratification might guide us to eventually develop a decision tool for identifying FBSS patients. Easing and helping diagnosis of FBSS should improve referral yield to specialists and accelerate patient flow through the care pathway. Hence, FBSS patients, who usually present a long standing history of pain, would have access to "appropriate" therapies earlier. This could lead to better outcomes. The aim of this multicentre, prospective study is to collect specific data that are not collected in routine in order to better define and understand the potential FBSS population and to accelerate the diagnostic and optimize the choice of appropriate treatment.

A multidisciplinary approach through a pain management clinical network, as it has been structured in Poitiers, will ensure that an exhaustive characterization of FBSS patients and their care pathway will be collected. In addition, since the cooperation between orthopaedic and neuro spine surgeons is not a common relationship found all over Europe (as it is observed in Poitiers), this study also aims to better understand the development of interactions between physicians/professionals and the substantial advantage which would result from bridging this gap. The N3MT (NeuroMapping Tools) software developed in Poitiers to collect data and assess objectively pain surface and intensity changes, before/after any treatment, with quantitative measurements, will be used as the central key of this project.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2016-11-07
• Study First Submitted QC: 2016-11-14
• Study First Posted: 2016-11-15
• Study Start: 2017-01
• Primary Completion: 2019-05-16
• Study Completion: 2019-05-31
• Status Verified: 2019-07
• Last Update Submitted: 2019-07-03
• Last Update Posted: 2019-07-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

• Patient has signed and dated the Informed Consent Form.
• Patient is ≥ 18 years of age at time of "Informed Consent Form" signature.
• Patient had most recent back surgery more than 6 months ago.
• Patient has developed post-operative Chronic Back with or without Leg Pain (potential FBSS).
• Patient has persistent back pain for more than 6 months.
• Average low back or leg pain is ≥ 4 as assessed by the baseline NPRS.

Exclusion Criteria

• Patient has already a confirmed FBSS diagnosis.
• Patient is or has been treated with SCS, subcutaneous or peripheral nerve stimulation, an intrathecal drug delivery system.
• Investigator suspects substance abuse that might confound the study results.
• Patient has a life expectancy of less than 12 months beyond study enrollment.
• Patient is less than 18 years of age.
• Patient is pregnant or planning to become pregnant during the course of the study.
• Patient is unable to undergo study assessments or complete questionnaires independently (e.g., is illiterate).
• Patient is a member of a vulnerable population.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Follow-up patient	No name	Medical follow-up visit

Primary Outcome Measures

Name	Time	Method
Incidence of clinical diagnosis of FBSS	12 month-follow up visit	Incidence of clinical diagnosis of FBSS in the broad population of post-surgical pain syndrome, identified by multidisciplinary team of independent experts (1 pain physician, 1 neurosurgeon and 1 psychiatric), with morphological and clinical characterization of the syndrome.

Secondary Outcome Measures

Name	Time	Method
Pain intensity (NRPS)	Initial visit and 3 month, 6 month, 9 month and 12 month-follow up Visits	* Reduction of the NRPS score measuring pain intensity: Global pain, Back pain and Leg pain.; * Proportion of patients with NRPS score \< 4.; * Proportion of patients obtaining a reduction ≥ 25%, 50% and 75%: Global pain, Back pain and Leg pain NRPS.
Quality of life (EQ5D)	Initial visit and 3 month, 6 month, 9 month and 12 month-follow up Visits
Psychological State (HADS)	Initial visit and 3 month, 6 month, 9 month and 12 month-follow up Visits
Pain Catastrophizing Scale (PCS CF)	Initial visit and 3 month, 6 month, 9 month and 12 month-follow up Visits
Functional capacity (ODI)	Initial visit and 3 month, 6 month, 9 month and 12 month-follow up Visits
Pain surface and intensity (Mapping Tool)	Initial visit and 3 month, 6 month, 9 month and 12 month-follow up Visits	* Reduction of the Global Pain Surface measured on the NeuroPain't module of the software, during treatment, before/after a therapeutic strategy is used.; * Reduction of pain intensities associated with the quantitative surface measurements.; * Reduction of the mechanical/neuropathic component of objective pain.
Adverse Events/ Serious Adverse Events	Initial visit and 3 month, 6 month, 9 month and 12 month-follow up Visits

Trial Locations

Locations (1)

Poitiers Hospital University; 🇫🇷 Poitiers, France