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Subperception dorsal root ganglion stimulation versus sham stimulation in established responders: a randomized, double-blind crossover clinical trial
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.ORCID iD: 0000-0003-2912-7059
Umeå University, Faculty of Medicine, Department of Diagnostics and Intervention.ORCID iD: 0000-0002-4874-6800
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.
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2026 (English)In: Regional anesthesia and pain medicine, ISSN 1098-7339, E-ISSN 1532-8651Article in journal (Refereed) Epub ahead of print
Abstract [en]

Background: subperception (paresthesia-free) dorsal root ganglion (DRG) stimulation is increasingly used for focal neuropathic pain, but sham-controlled evidence remains limited. We conducted a randomized, double-blind, sham-controlled crossover trial with enriched enrollment design in established DRG-stimulation responders.

Methods: In this single-center trial, adults with chronic peripheral neuropathic or nociplastic pain with implanted DRG system and sustained response (≥50% pain reduction for ≥3 months on stable stimulation settings and medication) were randomized 1:1 to active→sham or sham→active stimulation. Participants completed two 5-day treatment periods separated by a 24-hour washout with stimulation off. Active stimulation was delivered at 90% of the perception threshold, and sham was stimulation off. The primary outcome was median pain intensity on a 0–10 Numeric Rating Scale (NRS). Secondary outcomes included patient satisfaction and Patient Global Impression of Change (PGIC) domains. Analyses used Wilcoxon signed-rank tests with Hodges-Lehmann estimates.

Results: In 20 randomized patients, pain intensity was lower during active than sham stimulation (median NRS 3.0 (IQR 2.0–4.0) vs 6.0 (IQR 4.0–7.0); Hodges-Lehmann median difference, −2.5; 95% CI −3.0 to −2.0; p<0.001). Patient satisfaction and all PGIC domains favored active stimulation. Two participants terminated one treatment period early per prespecified criteria; available data were retained. No serious or device-related adverse events were reported.

Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2026.
National Category
Neurosciences
Research subject
Neurosurgery
Identifiers
URN: urn:nbn:se:umu:diva-253252DOI: 10.1136/rapm-2026-107906PubMedID: 42128597Scopus ID: 2-s2.0-105038893618OAI: oai:DiVA.org:umu-253252DiVA, id: diva2:2060352
Available from: 2026-05-18 Created: 2026-05-18 Last updated: 2026-05-25

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Tabatabaei, PedramWänman, JohanAwad, AmarSjöberg, Rickard L.Hariz, MarwanBlomstedt, Patric

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Tabatabaei, PedramWänman, JohanAwad, AmarBredemo, LindaSjöberg, Rickard L.Hariz, MarwanBlomstedt, Patric
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NeurosciencesDepartment of Diagnostics and Intervention
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