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Published on: October 7, 2017
Subperception dorsal root ganglion stimulation versus sham stimulation in established responders: a randomized,
Pedram Tabatabaei1, Johan Wänman2, Amar Awad3
1Department of Clinical Science, Neurosciences, Umea Universitet, Umeå, Sweden pedram.tabatabaei@umu.se.
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.
Conclusions:
In established DRG responders, subperception DRG stimulation produced clinically meaningful pain reduction and improved patient-reported outcomes compared with sham. These findings support efficacy during the maintenance phase of treatment, but their generalizability to unselected chronic pain populations or earlier treatment phases is limited.
Trial Registration Number:
NCT07170722.

