Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Transcutaneous Vagus Nerve Stimulation for Pain and Autonomic Dysfunction in Fibromyalgia (RESET-FMS) (RESET-FMS)

30 de junho de 2026 atualizado por: Andrea Truini, University of Roma La Sapienza

RESET-FMS: A Randomized Sham-Controlled Trial of Transcutaneous Vagus Nerve Stimulation for Pain, Autonomic Dysfunction, and Fatigue in Patients With Fibromyalgia Syndrome

Fibromyalgia syndrome (FMS) is a chronic pain condition characterized by widespread pain, fatigue, sleep disturbances, cognitive symptoms, and autonomic dysfunction, significantly impairing quality of life. Increasing evidence suggests that, beyond central pain dysregulation, patients with FMS frequently exhibit autonomic nervous system dysfunction, characterized by sympathetic nervous system (SNS) hyperactivity at rest, with reduced SNS recruitment during orthostatic challenge. Moreover, approximately 50% of patients with FMS show reduced intraepidermal small fiber density on skin biopsy, a condition referred to as small fiber pathology (SFP), which has recently been suggested to contribute to autonomic dysfunction in these patients. Despite currently available pharmacological and non-pharmacological treatments, therapeutic efficacy remains limited, highlighting the need for novel mechanism-based interventions.

Transcutaneous vagus nerve stimulation (tVNS) is a non-invasive neuromodulation technique that enhances parasympathetic activity through stimulation of the auricular branch of the vagus nerve. Preliminary studies suggest that tVNS may improve pain, autonomic symptoms, mood, and quality of life in patients with FMS, although available evidence is limited by small sample sizes and heterogeneous methodologies.

The RESET-FMS study is a randomized, sham-controlled, double-blind clinical trial designed to evaluate the efficacy of tVNS in patients with FMS. Participants will be randomized in a 1:1 ratio to receive either active tVNS or sham stimulation for four consecutive weeks. Stimulation will be administered daily for 30 minutes using the Nurosym™ device applied at the tragus of the external ear.

The primary objective is to assess the effect of active tVNS compared with sham stimulation on fibromyalgia severity, measured by the revised Fibromyalgia Impact Questionnaire (rFIQ) at the end of treatment (T4), adjusted for baseline values.

Exploratory objectives include:

  • evaluation of autonomic symptoms, fatigue, pain distribution, symptom severity, and sleep quality using validated clinical scales, including the Composite Autonomic Symptom Score (COMPASS-31), Fatigue Severity Scale (FSS), Widespread Pain Index (WPI), Symptom Severity Score (SSS), and Pittsburgh Sleep Quality Index (PSQI) at T4;
  • assessment of the persistence of treatment effects four weeks after treatment discontinuation (T8);
  • evaluation of treatment effects during intermediate assessments (T2);
  • evaluation of the effects of tVNS on non-invasive indices of autonomic nervous system function, including heart rate variability (HRV) and sudomotor function assessed by dynamic sweat test (DST);
  • analysis of serum biomarkers potentially associated with autonomic dysfunction, neuroinflammation, and cognitive symptoms, including neuropeptide Y (NPY), interleukin-6 (IL-6), and neurofilament light chain (NFL);
  • comparison of treatment response between patients with and without evidence of small-fiber pathology on skin biopsy;
  • identification of clinical and biological predictors of response to tVNS. The study is expected to provide clinically relevant evidence regarding the efficacy and safety of tVNS in FMS and to improve the understanding of the relationship between pain modulation, autonomic dysfunction, and peripheral nervous system involvement in this condition. The identification of predictors of treatment response may contribute to the development of more personalized therapeutic strategies for patients with FMS.

Visão geral do estudo

Descrição detalhada

Fibromyalgia syndrome (FMS) is a chronic pain condition characterized by widespread pain associated with fatigue, sleep disturbances, cognitive symptoms, mood alterations, and autonomic dysfunction, leading to substantial impairment in quality of life and daily functioning. Current evidence supports the concept of FMS as a nociplastic pain disorder, in which altered central pain processing and impaired descending pain modulation play a key pathophysiological role. However, increasing evidence suggests that peripheral nervous system involvement and autonomic nervous system dysfunction may also contribute significantly to symptom generation and clinical heterogeneity in this condition.

Several studies have demonstrated that patients with FMS frequently exhibit cardiovascular autonomic dysfunction, characterized by sympathetic nervous system hyperactivity at rest and impaired autonomic adaptive responses during orthostatic challenge. These abnormalities have been documented through heart rate variability (HRV) analysis and other autonomic function tests and have been associated with orthostatic intolerance symptoms, fatigue, and pain severity. In addition, approximately 50% of patients with fibromyalgia show evidence of reduced intraepidermal nerve fiber density on skin biopsy, a condition referred to as small fiber pathology (SFP). Recent findings suggest that small fiber involvement in FMS non è limitato alle piccole fibre somatiche, ma anche alle fibre autonomiche simpatiche post- gangliari. Il ruolo della SFP nella FMS è ancora sconosciuto, tuttavia un recente studio ha dimostrato come la SFP contribuisca alla disfunzione autonomica nella FMS.

Despite the availability of pharmacological and non-pharmacological therapeutic approaches, including antidepressants, gabapentinoids, physical therapy, and psychological interventions, treatment efficacy in FMS remains limited. Consequently, there is growing interest in mechanism-based neuromodulation strategies targeting autonomic dysfunction and central pain modulation pathways.

Transcutaneous vagus nerve stimulation (tVNS) is a non-invasive neuromodulation technique designed to stimulate the auricular branch of the vagus nerve through cutaneous electrical stimulation applied to specific regions of the external ear. By enhancing parasympathetic activity and modulating central autonomic and pain-processing networks, tVNS has emerged as a promising therapeutic strategy for chronic pain disorders and conditions associated with autonomic imbalance. Preliminary studies in FMS suggest that tVNS may improve pain, autonomic symptoms, mood, and quality of life; however, currently available studies are limited by relatively small sample sizes and heterogeneous methodologies.

The RESET-FMS study is a randomized, sham-controlled, double-blind clinical trial designed to evaluate the efficacy of transcutaneous vagus nerve stimulation in female patients with fibromyalgia syndrome and to investigate clinical and biological predictors of treatment response.

Female participants meeting the diagnostic criteria for fibromyalgia according to the 2016 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification criteria will be enrolled and randomized to receive either active tVNS or sham stimulation. Randomization will be computer-generated with variable block sizes in order to ensure allocation concealment and balance between groups throughout the enrollment period. Both participants and outcome assessors will remain blinded to treatment allocation.

The intervention will consist of daily 30-minute stimulation sessions administered for four consecutive weeks using the Nurosym™ device applied at the tragus of the external ear. Participants allocated to the active treatment group will receive standard transcutaneous vagus nerve stimulation, whereas the sham group will undergo identical procedures using a stimulation modality that does not deliver a therapeutic vagal stimulation pattern.

The primary objective of the study is to assess the efficacy of active tVNS compared with sham stimulation on fibromyalgia severity, measured by the revised Fibromyalgia Impact Questionnaire (rFIQ) at the end of treatment (T4), adjusted for baseline values.

Exploratory objectives include:

  • evaluation of autonomic symptoms, fatigue, pain distribution, symptom severity, and sleep quality using validated clinical scales, including the Composite Autonomic Symptom Score (COMPASS-31), Fatigue Severity Scale (FSS), Widespread Pain Index (WPI), Symptom Severity Score (SSS), and Pittsburgh Sleep Quality Index (PSQI);
  • assessment of the persistence of treatment effects four weeks after treatment discontinuation (T8);
  • evaluation of treatment effects during intermediate assessment (T2);
  • comparison of treatment response between patients with and without evidence of small fiber pathology on skin biopsy;
  • evaluation of the effects of tVNS on non-invasive indices of autonomic nervous system function, including heart rate variability (HRV) and sudomotor function assessed by dynamic sweat test (DST);
  • evaluation of changes in serum biomarkers potentially associated with autonomic dysfunction and neuroinflammation following tVNS treatment, including neuropeptide Y (NPY), interleukin-6 (IL-6), and neurofilament light chain (NFL);
  • identification of clinical and biological predictors of response to tVNS. Clinical assessments will be performed at baseline, during treatment, at the end of treatment, and during follow-up evaluations. Participants will complete validated questionnaires assessing fibromyalgia severity, autonomic symptoms, fatigue, sleep quality, and symptom burden. Cardiovascular autonomic function will be assessed through ECG-derived HRV analysis, including spectral analysis of R-R interval variability. Skin biopsy will be performed at baseline to evaluate intraepidermal nerve fiber density and morphological evidence of small fiber pathology. Blood samples collected at baseline and at the end of treatment will be used for serum biomarker analysis.

Statistical analyses will be conducted according to the intention-to-treat principle. The primary endpoint will be analyzed using mixed-effects models for repeated measures with adjustment for baseline values. Exploratory analyses will evaluate treatment effects on autonomic function parameters and biomarker levels, as well as predictors of clinical response. Additional subgroup analyses will compare treatment response in patients with and without evidence of small fiber pathology.

The study is expected to provide clinically relevant evidence regarding the efficacy and safety of transcutaneous vagus nerve stimulation in fibromyalgia syndrome and to improve understanding of the relationship between autonomic dysfunction, peripheral nervous system involvement, and nociplastic pain mechanisms in this condition. Furthermore, the identification of predictors of response to vagal neuromodulation may contribute to the development of more personalized therapeutic strategies for patients with fibromyalgia.

Tipo de estudo

Intervencional

Inscrição (Estimado)

80

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Lazio
      • Rome, Lazio, Itália, 00185
        • Recrutamento
        • Department of Human Neuroscience
        • Contato:
        • Investigador principal:
          • Andrea Truini, MD, PhD
        • Subinvestigador:
          • Pietro Falco, MD, PhD
        • Subinvestigador:
          • Eleonora Galosi, MD, PhD
        • Subinvestigador:
          • Caterina Maria Leone, MD, PhD
        • Subinvestigador:
          • Giuseppe Di PIetro, MD, PhD
        • Subinvestigador:
          • Giulia Di Stefano, MD, PhD
        • Subinvestigador:
          • Manuela Di Franco, MD, PhD
        • Subinvestigador:
          • Cristina Iannuccelli, MD, PhD
        • Subinvestigador:
          • Giulio Dolcini, MD, PhD
        • Subinvestigador:
          • Martina Favretti, MD, PhD

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Diagnosis of fibromyalgia syndrome according to the 2016 ACR/EULAR classification criteria;
  • Stable pharmacological treatment for at least 1 month before enrollment;
  • Ability to understand and complete study procedures and questionnaires;
  • Ability to provide written informed consent.

Exclusion Criteria:

  • Presence of an active implantable medical device or any implanted metallic or electronic device near the ear or heart;
  • History of severe coronary artery disease or myocardial infarction;
  • Heart failure classified as New York Heart Association (NYHA) class II-IV;
  • Cardiac arrhythmias or severe bradycardia;
  • Carotid artery atherosclerosis;
  • Chronic kidney disease stage II or higher;
  • Concomitant immune-mediated rheumatic disease;
  • Pregnancy;
  • Active malignancy or previous malignancy not in remission;
  • Ongoing infection;
  • Changes in pharmacological treatment within 1 month before enrollment;
  • Concomitant central or peripheral nervous system disorders, except isolated small-fiber pathology on skin biopsy;
  • Cognitive impairment detected during neurological examination;
  • Severe psychiatric comorbidities requiring specific treatment;
  • Pain caused by other medical conditions that cannot be distinguished from fibromyalgia-related pain;
  • Current or previous alcohol or substance abuse;
  • Inadequate understanding of the Italian language.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Active Transcutaneous Vagus Nerve Stimulation
Participants assigned to this arm will receive active transcutaneous vagus nerve stimulation (tVNS) using the Nurosym™ device applied at the tragus of the external ear. Stimulation sessions will last 30 minutes and will be administered once daily for four consecutive weeks. Stimulation intensity will be individually adjusted by participants until a mild tingling sensation is perceived at the stimulation site. The device delivers an active therapeutic vagal stimulation pattern intended to modulate autonomic nervous system activity and pain processing pathways.
Transcutaneous vagus nerve stimulation (tVNS) will be delivered using the Nurosym™ device applied at the tragus of the external ear. Participants will undergo one 30-minute stimulation session daily for four consecutive weeks. Stimulation intensity will be individually adjusted until a mild tingling sensation is perceived at the stimulation site. The intervention is designed to activate the auricular branch of the vagus nerve and modulate autonomic nervous system activity and pain-processing pathways.
Comparador Falso: Sham Transcutaneous Vagus Nerve Stimulation
Participants assigned to this arm will receive sham transcutaneous vagus nerve stimulation using the Nurosym™ device applied at the tragus of the external ear. Sham stimulation sessions will last 30 minutes and will be administered once daily for four consecutive weeks. Participants will follow the same procedures used for active stimulation, including adjustment of stimulation intensity until a mild tingling sensation is perceived. However, after the session is initiated, the device will automatically reduce stimulation output to zero within a few seconds, without delivering an active therapeutic vagal stimulation pattern.
Sham transcutaneous vagus nerve stimulation will be delivered using the Nurosym™ device applied at the tragus of the external ear. Participants will undergo one 30-minute session daily for four consecutive weeks and will follow the same procedures used for active stimulation, including adjustment of stimulation intensity until a mild tingling sensation is perceived. However, after initiation of the session, the device will automatically reduce stimulation output to zero within a few seconds and will not deliver an active therapeutic vagal stimulation pattern.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in Revised Fibromyalgia Impact Questionnaire (rFIQ) Score at Week 4
Prazo: From baseline to end of treatment at Week 4
The primary outcome measure will be the difference between active transcutaneous vagus nerve stimulation and sham stimulation in the change from baseline to Week 4 in the revised Fibromyalgia Impact Questionnaire (rFIQ) score. The rFIQ is a validated questionnaire assessing the overall impact of fibromyalgia on daily functioning and symptom severity, with higher scores indicating greater disease burden. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to end of treatment at Week 4

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Change in COMPASS-31 questionnaire at Week 4
Prazo: From baseline to end of treatment at Week 4
Change from baseline to Week 4 in autonomic symptom burden measured using the Composite Autonomic Symptom Score (COMPASS-31). The questionnaire will be administered electronically through a REDCap-based application. Higher scores indicate greater autonomic symptom severity.
From baseline to end of treatment at Week 4
Change in Sudomotor Function at Week 4
Prazo: From baseline to end of treatment at Week 4
Changes in sudomotor function will be assessed using dynamic sweat testing (DST) performed at baseline and Week 4. DST will be used as a non-invasive measure of autonomic small-fiber function by evaluating sweat production and sudomotor responses.
From baseline to end of treatment at Week 4
Change in Serum Biomarker Levels at Week 4
Prazo: From baseline to the end of Week 4
Changes in serum biomarkers potentially associated with autonomic dysfunction and neuroinflammation will be assessed between baseline and Week 4. Serum levels of neuropeptide Y (NPY), interleukin-6 (IL-6), and neurofilament light chain (NFL) will be measured using commercially available ELISA assays.
From baseline to the end of Week 4
Change in Revised Fibromyalgia Impact Questionnaire (FIQR) Score at Week 2
Prazo: From baseline to Week 2
Change from baseline to Week 2 in fibromyalgia-related health status measured using the Revised Fibromyalgia Impact Questionnaire (FIQR). Higher scores indicate greater disease impact and functional impairment. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 2
Change in Widespread Pain Index (WPI) Score at Week 4
Prazo: From baseline to end of treatment at Week 4
Change from baseline to Week 4 in pain distribution measured using the Widespread Pain Index (WPI). Higher scores indicate a greater number of painful body regions. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to end of treatment at Week 4
Change in Symptom Severity Score (SSS) at Week 4
Prazo: From baseline to end of treatment at Week 4
Change from baseline to Week 4 in symptom severity measured using the Symptom Severity Score (SSS). Higher scores indicate greater severity of fibromyalgia-related symptoms. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to end of treatment at Week 4
Change in Pittsburgh Sleep Quality Index (PSQI) Score at Week 4
Prazo: From baseline to end of treatment at Week 4
Change from baseline to Week 4 in sleep quality measured using the Pittsburgh Sleep Quality Index (PSQI). Higher scores indicate poorer sleep quality. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to end of treatment at Week 4
Change in Fatigue Severity Scale (FSS) Score at Week 4
Prazo: From baseline to end of treatment at Week 4
Change from baseline to Week 4 in fatigue severity measured using the Fatigue Severity Scale (FSS). Higher scores indicate greater fatigue severity. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to end of treatment at Week 4
Change in COMPASS-31 Score at Week 2
Prazo: From baseline to Week 2
Change from baseline to Week 2 in autonomic symptom burden measured using the Composite Autonomic Symptom Score (COMPASS-31). Higher scores indicate greater autonomic symptom severity. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 2
Change in Widespread Pain Index (WPI) Score at Week 2
Prazo: From baseline to Week 2
Change from baseline to Week 2 in pain distribution measured using the Widespread Pain Index (WPI). Higher scores indicate a greater number of painful body regions. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 2
Change in Symptom Severity Score (SSS) at Week 2
Prazo: From baseline to Week 2
Change from baseline to Week 2 in the Symptom Severity Score (SSS), a measure of the severity of core fibromyalgia symptoms, including fatigue, unrefreshing sleep, cognitive symptoms, and other somatic symptoms. Higher scores indicate greater symptom severity. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 2
Change in Pittsburgh Sleep Quality Index (PSQI) Score at Week 2
Prazo: From baseline to Week 2
Change from baseline to Week 2 in sleep quality measured using the Pittsburgh Sleep Quality Index (PSQI). Higher scores indicate poorer sleep quality. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 2
Change in Fatigue Severity Scale (FSS) Score at Week 2
Prazo: From baseline to Week 2
Change from baseline to Week 2 in fatigue severity measured using the Fatigue Severity Scale (FSS). Higher scores indicate greater fatigue severity. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 2
Change in Revised Fibromyalgia Impact Questionnaire (FIQR) Score at Week 8
Prazo: From baseline to Week 8
Change from baseline to Week 8 in fibromyalgia-related health status measured using the Revised Fibromyalgia Impact Questionnaire (FIQR). Higher scores indicate greater disease impact and functional impairment. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 8
Change in COMPASS-31 Score at Week 8
Prazo: From baseline to Week 8
Change from baseline to Week 8 in autonomic symptom burden measured using the Composite Autonomic Symptom Score (COMPASS-31). Higher scores indicate greater autonomic symptom severity. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 8
Change in Widespread Pain Index (WPI) Score at Week 8
Prazo: From baseline to Week 8
Change from baseline to Week 8 in pain distribution measured using the Widespread Pain Index (WPI). Higher scores indicate a greater number of painful body regions. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 8
Change in Symptom Severity Score (SSS) at Week 8
Prazo: From baseline to Week 8
Change from baseline to Week 8 in the Symptom Severity Score (SSS), a measure of the severity of core fibromyalgia symptoms, including fatigue, unrefreshing sleep, cognitive symptoms, and other somatic symptoms. Higher scores indicate greater symptom severity. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 8
Change in Pittsburgh Sleep Quality Index (PSQI) Score at Week 8
Prazo: From baseline to Week 8
Change from baseline to Week 8 in sleep quality measured using the Pittsburgh Sleep Quality Index (PSQI). Higher scores indicate poorer sleep quality. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 8
Change in Fatigue Severity Scale (FSS) Score at Week 8
Prazo: From baseline to Week 8
Change from baseline to Week 8 in fatigue severity measured using the Fatigue Severity Scale (FSS). Higher scores indicate greater fatigue severity. Questionnaire data will be collected electronically using a REDCap-based application.
From baseline to Week 8
Change in Total Heart Rate Variability Power at Week 4
Prazo: From baseline to Week 4
Change from baseline to Week 4 in total heart rate variability power derived from electrocardiogram R-R interval recordings. Total power reflects overall heart rate variability across the analyzed frequency spectrum and is expressed in milliseconds squared (ms²).
From baseline to Week 4
Change in Low-Frequency Heart Rate Variability Power at Week 4
Prazo: From Baseline to Week 4
Change from baseline to Week 4 in low-frequency heart rate variability power derived from electrocardiogram R-R interval recordings. Low-frequency power is expressed in milliseconds squared (ms²).
From Baseline to Week 4
Change in Low-Frequency Heart Rate Variability in Normalized Units at Week 4
Prazo: From baseline to week 4
Change from baseline to Week 4 in low-frequency heart rate variability expressed in normalized units (LFnu), derived from electrocardiogram R-R interval recordings. Higher values indicate a greater relative contribution of low-frequency oscillations to heart rate variability.
From baseline to week 4
Change in LF/HF Ratio at Week 4
Prazo: From baseline to week 4
Change from baseline to Week 4 in the ratio between low-frequency and high-frequency heart rate variability components (LF/HF ratio), derived from electrocardiogram R-R interval recordings. The LF/HF ratio is a dimensionless measure of sympathovagal balance.
From baseline to week 4
Change in Total Heart Rate Variability Power at Week 8
Prazo: From baseline to week 8
Change from baseline to Week 8 in total heart rate variability power derived from electrocardiogram R-R interval recordings. Total power reflects overall heart rate variability across the analyzed frequency spectrum and is expressed in milliseconds squared (ms²).
From baseline to week 8
Change in Low-Frequency Heart Rate Variability Power at Week 8
Prazo: From baseline to week 8
Change from baseline to Week 8 in low-frequency heart rate variability power derived from electrocardiogram R-R interval recordings. Low-frequency power is expressed in milliseconds squared (ms²).
From baseline to week 8
Change in Low-Frequency Heart Rate Variability in Normalized Units at Week 8
Prazo: From baseline to week 8
Change from baseline to Week 8 in low-frequency heart rate variability expressed in normalized units (LFnu), derived from electrocardiogram R-R interval recordings. Higher values indicate a greater relative contribution of low-frequency oscillations to heart rate variability.
From baseline to week 8
Change in LF/HF Ratio at Week 8
Prazo: from baseline to week 8
Change from baseline to Week 8 in the ratio between low-frequency and high-frequency heart rate variability components (LF/HF ratio), derived from electrocardiogram R-R interval recordings. The LF/HF ratio is a dimensionless measure of sympathovagal balance.
from baseline to week 8

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Andrea Truini, MD, PhD, University of Roma La Sapienza

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

8 de junho de 2026

Conclusão Primária (Estimado)

25 de maio de 2027

Conclusão do estudo (Estimado)

30 de setembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

12 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

30 de junho de 2026

Primeira postagem (Real)

2 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

2 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

30 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • RESET-FMS-2026

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

De-identified individual participant data underlying the results reported in this study will be made available upon reasonable request to the corresponding investigator, following publication, for purposes of scientific research and after approval of a methodologically sound proposal.

Prazo de Compartilhamento de IPD

Beginning 6 months and ending 5 years following article publication.

Critérios de acesso de compartilhamento IPD

Researchers who provide a methodologically sound proposal. Proposals should be directed to the corresponding investigator. Data will be shared after approval of the proposal and execution of a data access agreement, in accordance with institutional and ethical regulations.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • ANALYTIC_CODE

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever