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Clinical Trials/NCT02774694
NCT02774694
Not yet recruiting
Not Applicable

Observational Study of the Nociceptive Flexion Reflex Threshold to Predict Outcome After Interventional Pain Management Procedures in Patients With Chronic Back and Neck Pain. A Study of Diagnostic Accuracy

Benno Rehberg-Klug0 sites350 target enrollmentJanuary 2026

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Benno Rehberg-Klug
Enrollment
350
Primary Endpoint
ROC-AUC for incidence of pain reduction>30% at 1 week
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Interventional pain management for back and neck pain is widely used, but the indications and relative merits of these techniques rest subject to discussion. This study aims to identify prognostic criteria for patients who might specifically benefit from interventional pain management. Specifically, the nociceptive reflex threshold will be investigated, which is a measure of central sensibilisation and thus a potentially important prognostic factor.

Detailed Description

Interventional pain management is resource-intensive and carries non-negligible risks. Not all patients profit equally from such procedures. For those who do not benefit, the risk of potential complications is futile, and the resources are wasted. Therefore, a possibility to distinguish responding patients from non-responders would be important. Central pain sensitization has been related to poor outcome, and electrical pain and reflex thresholds are a good measure of pain hypersensitivity at least in chronic low back pain. Especially the nociceptive flexion reflex (NFR) threshold has been identified to correlate well with central pain hypersensibility. Successful interventional pain treatment has been shown to reverse central hypersensibility as measured by the NFR threshold. NFR threshold, in contrast to pain threshold, seems to be a measure independent of psychological factors. Thus the NFR threshold could give information independent of psychological factors in order to predict poor outcome of interventional pain management procedures. The study will be a prospective observational trial of diagnostic accuracy.

Registry
clinicaltrials.gov
Start Date
January 2026
End Date
September 2027
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Benno Rehberg-Klug
Responsible Party
Sponsor Investigator
Principal Investigator

Benno Rehberg-Klug

Médecin adjoint agrégé

University Hospital, Geneva

Eligibility Criteria

Inclusion Criteria

  • patients with chronic low back or neck pain (duration \>3 months)
  • scheduled for the following interventions: epidural injection, facet block, medial branch block, facet radiofrequency denervation, spinal cord stimulator implantation

Exclusion Criteria

  • inability to understand the patient information or the study questionnaires
  • patients \<18 years old
  • patients with implanted pacemakers or defibrillators

Outcomes

Primary Outcomes

ROC-AUC for incidence of pain reduction>30% at 1 week

Time Frame: 1 week

Primary study outcome is the diagnostic accuracy of the NFR threshold, measured as area under the "receiver operating characteristic ROC" curve, for the following main pain management outcome: "pain reduction of 30% one week after the interventional procedure

Secondary Outcomes

  • ROC-AUC for patient rating of improvement and satisfaction at 1 week(1 week)
  • ROC-AUC for incidence of pain reduction>30% at 1 month(1 month)
  • ROC-AUC for emotional functioning at 1 week(1 week)
  • ROC-AUC for incidence of pain reduction>30% at 6 months(6 months)
  • adverse events of interventional pain management(1 week)
  • patient disposition at 1 week, 1,3, and 6 months(6 months)
  • ROC-AUC for incidence of pain reduction>30% at 3 months(3 months)
  • ROC-AUC for physical functioning at 1 week(1 week)

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