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Association of low-dose naltrexone and transcranial direct current stimulation in fibromyalgia: a randomized, double-blinded, parallel clinical trial

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dc.contributor.author Paula, Tania Maria Hendges de
dc.contributor.author Castro, Mariane Schäffer
dc.contributor.author Medeiros, Liciane Fernandes
dc.contributor.author Paludo, Rodrigo Hernandes
dc.contributor.author Couto, Fabricia Fritz
dc.contributor.author Costa, Tainá Ramires da
dc.contributor.author Fortes, Juliana Pereira
dc.contributor.author Salbego, Maiara de Oliveira
dc.contributor.author Behnck, Gabriel Schardosim
dc.contributor.author Moura, Thielly Amaral Mesquita de
dc.contributor.author Tarouco, Mariana Lenz
dc.contributor.author Caumo, Wolnei
dc.contributor.author Souza, Andressa de
dc.date.accessioned 2024-02-29T12:47:41Z
dc.date.available 2024-02-29T12:47:41Z
dc.date.issued 2022
dc.identifier.citation CASTRO, M. S. et al. Association of low-dose naltrexone and transcranial direct current stimulation in fibromyalgia: a randomized, double-blinded, parallel clinical trial. BRAZILIAN JOURNAL OF ANESTHESIOLOGY, p. xx, 2022. Disponível em: https://www.sciencedirect.com/science/article/pii/S010400142200104X?via%3Dihub Acesso em: 22 fev. 2024. pt_BR
dc.identifier.uri http://hdl.handle.net/11690/3835
dc.description.abstract Introduction: Fibromyalgia is a complex, generalized, and diffuse chronic musculoskeletal pain. Pharmacological approaches are widely used to relieve pain and increase quality of life. LowDose Naltrexone (LDN) was shown to increase the nociceptive threshold in patients with fibromyalgia. Transcranial Direct Current Stimulation (tDCS) is effective for pain management. Objective: The purpose of this study was to evaluate the analgesic and neuromodulatory effects of a combination of LDN and tDCS in patients with fibromyalgia. Methods: This was a randomized, double-blinded, parallel, placebo/sham-controlled trial (NCT04502251; RBR-7HK8N) in which 86 women with fibromyalgia were included, and written informed consent was obtained from them. The patients were allocated into four groups: LDN + tDCS (n = 21), LDN + tDCS Sham (n = 22), placebo + tDCS (n = 22), and placebo+tDCS Sham (n = 21). The LDN or placebo (p.o.) intervention lasted 26 days; in the last five sessions, tDCS was applied (sham or active, 20 min, 2 mA). The following categories were assessed: sociodemographic, Visual Analog Pain Scale (VAS), Pain Catastrophizing Scale (PCS), State-Trait Anxiety Inventory (STAI), Fibromyalgia Impact Questionnaire (FIQ), Beck Depression Inventory (BDI-II), Profile of Chronic Pain Scale (PCP:S), Pain Pressure Threshold (PPT), and Conditioned Pain Modulation (CPM). Blood samples were collected to analyze BDNF serum levels. Results: At baseline, no significant difference was found regarding all measurements. VAS pain was significantly reduced in the LDN + tDCS (p = 0.010), LDN + tDCS Sham (p = 0.001), and placebo+tDCS Sham (p = 0.009) groups. In the PCP:S, the LDN+tDCS group showed reduced pain frequency and intensity (p = 0.001), effect of pain on activities (p = 0.014) and emotions (p = 0.008). Depressive symptoms reduced after all active interventions (p > 0.001). Conclusion: Combined LDN+tDCS has possible benefits in reducing pain frequency and intensity; however, a placebo effect was observed in pain using VAS, and further studies should be performed to analyze the possible association. pt_BR
dc.publisher BRAZILIAN JOURNAL OF ANESTHESIOLOGY pt_BR
dc.subject Fibromyalgia pt_BR
dc.subject Naltrexone pt_BR
dc.subject Pain pt_BR
dc.subject Transcranial direct current stimulation pt_BR
dc.title Association of low-dose naltrexone and transcranial direct current stimulation in fibromyalgia: a randomized, double-blinded, parallel clinical trial pt_BR
dc.type Other pt_BR


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