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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[21]   First-Line Anlotinib Treatment for Soft-Tissue Sarcoma in Chemotherapy-Ineligible Patients: An Open-Label, Single-Arm, Phase 2 Clinical Trial [J].
Li, Tao ;
Dong, Ying ;
Wei, Yongzhong ;
Wang, Shoufeng ;
Liu, Yunxia ;
Chen, Jia ;
Xiong, Wenhua ;
Lin, Nong ;
Huang, Xin ;
Liu, Meng ;
Yan, Xiaobo ;
Ye, Zhaoming ;
Li, Binghao .
CLINICAL CANCER RESEARCH, 2024, 30 (19) :4310-4317
[22]   Efficiency and Toxicity of Imatinib Mesylate Combined with Atorvastatin Calcium in the Treatment of Steroid-Refractory Chronic Graft-versus-Host Disease: A Single-Center, Prospective, Single-Arm, Open-Label Study [J].
Chen, Ting ;
Li, Jiali ;
Wei, Xiao ;
Yao, Han ;
Zhu, Lidan ;
Liu, Jia ;
Liu, Yuqing ;
Wang, Ping ;
Feng, Yimei ;
Gao, Shichun ;
Liu, Huanfeng ;
Wang, Lu ;
Zhao, Lu ;
Gao, Li ;
Zhang, Cheng ;
Gao, Lei ;
Zhang, Xi ;
Kong, Peiyan .
ACTA HAEMATOLOGICA, 2024, 147 (05) :499-510
[23]   Efficacy of Ultrasound-Guided Platelet-Rich Plasma (PRP) Injection in Patients with Sacroiliac Joint Pain: A Single-Arm, Before and After, Open-Label Clinical Trial [J].
Khosromanesh, Maliheh ;
Alikarami, Sogol ;
Espahbodi, Ebrahim ;
Yekta, Reza Atef ;
Kamali, Koorosh ;
Majedi, Hossein .
ARCHIVES OF NEUROSCIENCE, 2025, 12 (01)
[24]   Neoadjuvant Cytoreductive Treatment With BRAF/MEK Inhibition of Prior Unresectable Regionally Advanced Melanoma to Allow Complete Surgical Resection, REDUCTOR A Prospective, Single-arm, Open-label Phase II Trial [J].
Blankenstein, Stephanie A. ;
Rohaan, Maartje W. ;
Klop, Willem Martin C. ;
van der Hiel, Bernies ;
van de Wiel, Bart A. ;
Lahaye, Max J. ;
Adriaansz, Sandra ;
Sikorska, Karolina ;
van Tinteren, Harm ;
Sari, Aysegul ;
Grijpink-Ongering, Lindsay G. ;
van Houdt, Winan J. ;
Wouters, Michel W. J. M. ;
Blank, Christian U. ;
Wilgenhof, Sofie ;
van Thienen, Johannes V. ;
van Akkooi, Alexander C. J. ;
Haanen, John B. A. G. .
ANNALS OF SURGERY, 2021, 274 (02) :383-389
[25]   Rucaparib in patients with BAP1-deficient or BRCA1-deficient mesothelioma (MiST1): an open-label, single-arm, phase 2a clinical trial [J].
Fennell, Dean A. ;
King, Amy ;
Mohammed, Seid ;
Branson, Amy ;
Brookes, Cassandra ;
Darlison, Liz ;
Dawson, Alan G. ;
Gaba, Aarti ;
Hutka, Margaret ;
Morgan, Bruno ;
Nicholson, Adrian ;
Richards, Cathy ;
Wells-Jordan, Peter ;
Murphy, Gavin James ;
Thomas, Anne .
LANCET RESPIRATORY MEDICINE, 2021, 9 (06) :593-600
[26]   Effectiveness of Etanercept Biosimilar Initiating for Etanercept-Naive Patients, Using Ultrasound, Clinical, and Biomarker Assessments in Outcomes of Real-World Therapy (ENPORT-NGSK Study): An Interventional, Multicenter, Open-Label, Single-Arm Clinical Trial [J].
Sumiyoshi, Remi ;
Kawashiri, Shin-ya ;
Shimizu, Toshimasa ;
Koga, Tomohiro ;
Kiya, Rieko ;
Tashiro, Shigeki ;
Kawazoe, Yurika ;
Sato, Shuntaro ;
Ueki, Yukitaka ;
Suzuki, Takahisa ;
Yoshitama, Tamami ;
Tada, Yoshifumi ;
Hosogaya, Naoki ;
Yamamoto, Hiroshi ;
Kawakami, Atsushi .
JOURNAL OF CLINICAL MEDICINE, 2025, 14 (05)
[27]   Switching from originator infliximab to biosimilar infliximab in Japanese patients with rheumatoid arthritis achieving clinical remission (the IFX-SIRIUS study I) Study protocol for an interventional, multicenter, open-label, single-arm and noninferiority clinical trial with clinical, ultrasound, and biomarker assessments [J].
Kawashiri, Shin-ya ;
Shimizu, Toshimasa ;
Sato, Shuntaro ;
Morimoto, Shimpei ;
Kawazoe, Yurika ;
Sumiyoshi, Remi ;
Hosogaya, Naoki ;
Fukushima, Chizu ;
Yamamoto, Hiroshi ;
Kawakami, Atsushi .
MEDICINE, 2020, 99 (30) :E21151
[28]   Assessment of real-life patient handling experience of AVT02 administered subcutaneously via autoinjector in patients with moderate to severe active rheumatoid arthritis: an open-label, single-arm clinical trial, then an extension phase of AVT02 administered with a prefilled syringe [J].
Damjanov, Nemanja ;
Kirvalidze, Nana ;
Kurashvili, Nana ;
Berti, Fausto ;
Steiger, Matjaz ;
Sobierska, Joanna ;
Guenzi, Eric ;
Otto, Hendrik ;
Sattar, Abid ;
Haliduola, Halimu N. ;
Edwald, Elin ;
Stroissnig, Heimo .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2023, 23 (08) :781-789