Adjunctive tonic motor activation enables opioid reduction for refractory restless legs syndrome: a prospective, open-label, single-arm clinical trial

被引:3
|
作者
Buchfuhrer, Mark J. [1 ]
Roy, Asim [2 ]
Rodriguez, Stephanye [3 ]
Charlesworth, Jonathan D. [3 ]
机构
[1] Stanford Univ, Sch Med, Stanford, CA USA
[2] Ohio Sleep Med Inst, Dublin, OH USA
[3] Noctrix Hlth Inc, Dept Clin Res, Pleasanton, CA 94566 USA
关键词
Bioelectronics; Neurological disorder; Neuromodulation; Peripheral nerve stimulation; Opioids; Rrestless legs syndrome; Sleep disorder; DOUBLE-BLIND; CHRONIC PAIN; SLEEP; AUGMENTATION; VALIDATION;
D O I
10.1186/s12883-023-03462-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundThere is a large population of restless legs syndrome (RLS) patients who are refractory to medication. Whereas experts recommend off-label opioids as an effective long-term treatment for refractory RLS, reducing opioid dose could substantially reduce side effects and risks. Tonic motor activation (TOMAC) is a nonpharmacological therapeutic device indicated for refractory RLS. Here, we investigated if TOMAC could enable opioid dose reduction for refractory RLS.MethodsThis prospective, open-label, single-arm clinical trial [NCT04698343] enrolled 20 adults taking <= 60 morphine milligram equivalents (MMEs) per day for refractory RLS. Participants self-administered 30-min TOMAC sessions bilaterally over the peroneal nerve when RLS symptoms presented. During TOMAC treatment, opioid dose was reduced iteratively every 2-3 weeks until Clinician Global Impression of Improvement (CGI-I) score relative to baseline exceeded 5. Primary endpoint was percent of participants who successfully reduced opioid dose >= 20% with CGI-I <= 5. Secondary endpoints included mean successful percent opioid dose reduction with CGI-I <= 5.ResultsOn average, participants were refractory to 3.2 medications (SD 1.6) and were taking a stable dose of opioids for 5.3 years (SD 3.9). Seventy percent of participants (70%, 14 of 20) successfully reduced opioid dose >= 20% with CGI-I <= 5. Mean percent opioid dose reduction with CGI-I <= 5 was 29.9% (SD 23.7%, n = 20) from 39.0 to 26.8 MME per day. Mean CGI-I score at the reduced dose was 4.0 (SD 1.4), indicating no change to RLS severity.ConclusionsFor refractory RLS, TOMAC enabled substantial opioid dose reduction without increased RLS symptoms. These results suggest that TOMAC has the potential to reduce the risk profile associated with opioid therapy for refractory RLS.Trial registrationClinicalTrials.gov trial number NCT04698343 registered on January 6, 2021.
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页数:11
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