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- Ensaio Clínico NCT07626983
Botulinum Toxin Type A Versus Local Anesthetic Injection for Chronic Neuroma Pain After Combat-Related Amputation (NEUROQUIET)
Botulinum Toxin Type A Versus Local Anesthetic Injection for Chronic Neuroma Pain After Combat-Related Amputation: A Multicenter Randomized Double-Blind Trial
Patients with combat-related amputations frequently experience persistent neuroma pain that may interfere with rehabilitation, prosthesis use, sleep, mobility, and quality of life. Current treatment options often provide only temporary relief. This study aims to compare two ultrasound-guided injection approaches for chronic neuroma pain after combat-related amputation: botulinum toxin type A and local anesthetic injection.
Participants will be randomly assigned to receive one of the two treatments. Pain intensity, neuropathic pain symptoms, phantom limb pain, prosthesis tolerance, and functional outcomes will be evaluated during follow-up visits over a 24-week period.
The goal of the study is to determine whether botulinum toxin type A provides longer-lasting pain reduction and improved functional recovery compared with local anesthetic injection in patients with chronic neuroma pain after combat-related amputation.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Neuroma pain is a common and disabling complication after combat-related limb amputation. Persistent neuroma pain may contribute to residual limb pain, phantom limb pain, impaired prosthesis tolerance, sleep disturbance, reduced mobility, and decreased quality of life. Conventional treatment strategies, including local anesthetic injections, often provide only temporary pain relief.
Botulinum toxin type A has emerged as a potential treatment option because of its ability to modulate peripheral nociceptive signaling, reduce neurogenic inflammation, and decrease peripheral sensitization. However, evidence regarding its efficacy in patients with combat-related amputations remains limited.
The NEUROQUIET Trial is a multicenter, randomized, double-blind clinical trial designed to compare ultrasound-guided botulinum toxin type A injection versus ultrasound-guided local anesthetic injection for persistent neuroma pain after combat-related amputation.
Eligible participants with ultrasound-confirmed painful neuroma will be randomized in a 1:1 ratio to receive either botulinum toxin type A or local anesthetic injection under ultrasound guidance. Participants, outcome assessors, and data analysts will remain blinded to treatment allocation.
Patients will undergo longitudinal follow-up for 24 weeks. Outcomes will include pain intensity, neuropathic pain characteristics, phantom limb pain, residual limb pain, prosthesis tolerance, analgesic consumption, sleep disturbance, and patient-reported global improvement.
The study aims to determine whether botulinum toxin type A provides greater and longer-lasting analgesia compared with local anesthetic injection in patients with chronic neuroma pain following combat-related amputation.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Contato de estudo
- Nome: Dmytro Dmytriiev, PhD.Professor
- Número de telefone: +380674309449
- E-mail: mddmytriiev@gmail.com
Locais de estudo
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Vinnitsa, Ucrânia, 21000
- Vinnitsya university hospital
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Contato:
- Dmytro Dmytriiev, Phd
- Número de telefone: 0674309449
- E-mail: mddmytriiev@gmail.com
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Vinnytsia Oblast
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Kyiv, Vinnytsia Oblast, Ucrânia, 03143
- Feofaniya Clinical Hospital
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Contato:
- Andrii Khomenko, MD
- Número de telefone: +380937635858
- E-mail: farmen@ukr.net
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Age ≥18 years
- Combat-related limb amputation
- Persistent neuroma pain lasting ≥3 months
- Ultrasound-confirmed neuroma
- Positive Tinel sign over the neuroma
- Average pain intensity ≥4/10 on the Numeric Rating Scale (NRS)
- Stable analgesic regimen for at least 14 days before enrollment
- Ability to provide written informed consent
Exclusion Criteria:
- Active infection at the injection site
- Previous botulinum toxin injection within 6 months
- Previous neuroma surgery within 3 months
- Severe uncontrolled psychiatric disorder
- Coagulopathy or anticoagulant therapy contraindicating injection
- Known allergy to botulinum toxin or local anesthetics
- Severe uncontrolled systemic disease
- Inability to complete study follow-up or questionnaires
Plano de estudo
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 |
|---|---|
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Experimental: Botulinum Toxin Type A
Ultrasound-guided perineuroma injection of botulinum toxin type A for persistent neuroma pain after combat-related amputation.
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Ultrasound-guided perineuroma injection of botulinum toxin type A for treatment of persistent neuroma pain after combat-related amputation.
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Comparador Ativo: Local Anesthetic
Ultrasound-guided perineuroma injection of local anesthetic for persistent neuroma pain after combat-related amputation.
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Ultrasound-guided perineuroma injection of local anesthetic for treatment of persistent neuroma pain after combat-related amputation.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Change in neuroma pain intensity measured
Prazo: Baseline to 12 weeks after intervention
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Assessment of change in average neuroma pain intensity using an 11-point Numeric Rating Scale (0 = no pain, 10 = worst imaginable pain) following ultrasound-guided injection treatment.
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Baseline to 12 weeks after intervention
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Residual Limb Pain Intensity Assessed Using the Numeric Rating Scale (NRS)
Prazo: Baseline to 24 weeks
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Residual limb pain intensity will be assessed using the 11-point Numeric Rating Scale (NRS). Participants will rate their average residual limb pain during the previous 7 days on a scale from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst imaginable pain." Higher scores indicate greater pain intensity and a worse clinical outcome. Scale Information: Numeric Rating Scale (NRS) Minimum Value: 0 Maximum Value: 10 Interpretation: Higher scores indicate worse residual limb pain intensity. |
Baseline to 24 weeks
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Pain Catastrophizing
Prazo: Baseline, 3 months, 6 months, and 12 months after amputation.
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Pain catastrophizing will be assessed using the Pain Catastrophizing Scale (PCS), a validated 13-item self-report questionnaire designed to measure catastrophic thinking related to pain. The PCS evaluates three domains: rumination, magnification, and helplessness. Total scores range from 0 to 52, with higher scores indicating greater levels of pain catastrophizing and a worse psychological pain profile. Scale Information: Pain Catastrophizing Scale (PCS) Minimum Value: 0 Maximum Value: 52 Interpretation: Higher scores indicate greater pain catastrophizing and worse pain-related psychological outcomes. |
Baseline, 3 months, 6 months, and 12 months after amputation.
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Prosthesis Tolerance Assessed Using the Prosthesis Evaluation Questionnaire (PEQ) - Utility and Satisfaction Domains
Prazo: Baseline to 24 weeks
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Prosthesis tolerance will be assessed using selected domains of the Prosthesis Evaluation Questionnaire (PEQ), a validated instrument evaluating comfort, utility, satisfaction, and functional use of the prosthesis. Scores range from 0 to 100, with higher scores indicating better prosthesis tolerance and satisfaction. Scale Information: Prosthesis Evaluation Questionnaire (PEQ) Minimum Value: 0 Maximum Value: 100 Interpretation: Higher scores indicate better prosthesis tolerance, comfort, and prosthetic adaptation. |
Baseline to 24 weeks
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Analgesic Consumption
Prazo: Baseline to 24 weeks
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Analgesic consumption will be assessed by calculating the total daily analgesic use and converting opioid medications into Oral Morphine Equivalent Daily Dose (OMEDD). Non-opioid analgesics (e.g., acetaminophen, NSAIDs, gabapentinoids) will also be recorded. Higher opioid consumption indicates greater analgesic requirements and potentially more severe pain. Measurement: Oral Morphine Equivalent Daily Dose (OMEDD), expressed in milligrams per day (mg/day) Minimum Value: 0 mg/day Maximum Value: No predefined maximum value Interpretation: Higher values indicate greater analgesic consumption and higher pain management requirements. |
Baseline to 24 weeks
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Patient Global Impression of Change (PGIC)
Prazo: Week 12 and Week 24
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Overall perceived improvement will be assessed using the Patient Global Impression of Change (PGIC) scale. The PGIC is a validated patient-reported outcome measure that evaluates a participant's perception of change in pain, function, and overall health status since the beginning of treatment. Participants rate their overall improvement on a 7-point scale ranging from "Very much worse" to "Very much improved." Scale Information: Patient Global Impression of Change (PGIC) Minimum Value: 1 (Very much worse) Maximum Value: 7 (Very much improved) Interpretation: Higher scores indicate greater perceived improvement and better overall clinical outcomes. Scale Categories:
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Week 12 and Week 24
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Adverse Events
Prazo: Baseline to 24 weeks
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Adverse events will be assessed by recording the occurrence, type, severity, and relationship to treatment throughout the study period. Events may include medication-related adverse effects, prosthesis-related complications, falls, skin breakdown, residual limb complications, infections, hospitalizations, and other clinically significant events. Severity will be graded according to the Common Terminology Criteria for Adverse Events (CTCAE), Version 5.0, when applicable. Measurement: Number of participants experiencing one or more adverse events. Minimum Value: 0 participants Maximum Value: Number of participants enrolled in the study Interpretation: Higher values indicate a greater incidence of adverse events and worse safety outcomes. Additional Safety Assessment: Severity of adverse events will be categorized as Grade 1 (Mild) to Grade 5 (Death related to adverse event) according to CTCAE v5.0. |
Baseline to 24 weeks
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Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Sleep Disturbance
Prazo: Baseline to 24 weeks
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Sleep disturbance will be assessed using the Pittsburgh Sleep Quality Index (PSQI), a validated 19-item questionnaire that evaluates subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction during the previous month. The global PSQI score ranges from 0 to 21, with higher scores indicating poorer sleep quality and greater sleep disturbance. Scale Information: Pittsburgh Sleep Quality Index (PSQI) Minimum Value: 0 Maximum Value: 21 Interpretation: Higher scores indicate worse sleep quality and greater sleep disturbance. Clinical Interpretation: A global PSQI score >5 is commonly considered indicative of clinically significant sleep disturbance. |
Baseline to 24 weeks
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Functional Mobility
Prazo: Baseline to 24 weeks
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Functional mobility will be assessed using the Amputee Mobility Predictor (AMP), a validated performance-based instrument designed to evaluate ambulatory potential, balance, transfers, gait, and functional mobility in individuals with lower-limb amputation. The scale assesses the patient's ability to perform a series of mobility tasks and predicts prosthetic functional potential. Scale Information: Amputee Mobility Predictor (AMP) Minimum Value: 0 Maximum Value: 47 Interpretation: Higher scores indicate better functional mobility, greater ambulatory capacity, and improved rehabilitation outcomes. Clinical Interpretation: Higher AMP scores are associated with higher functional levels and greater potential for successful prosthetic use. |
Baseline to 24 weeks
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Need for Repeat Intervention
Prazo: Up to 24 weeks
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he need for repeat intervention will be assessed by recording the number of participants who require additional pain-related interventions following the initial treatment. Repeat interventions may include repeat nerve blocks, cryoneurolysis, radiofrequency ablation, neuroma surgery, revision procedures, additional injections, or other clinically indicated pain-management procedures. Measurement: Number of participants requiring one or more additional pain-related interventions during follow-up. Minimum Value: 0 participants Maximum Value: Number of participants enrolled in the study Interpretation: Higher values indicate a greater need for additional interventions and may reflect reduced durability or effectiveness of the initial treatment. Additional Analysis: Time to first repeat intervention (days) may also be recorded and analyzed as a secondary outcome. |
Up to 24 weeks
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Patient Satisfaction
Prazo: Week 12 and Week 24
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Patient satisfaction will be assessed using the Client Satisfaction Questionnaire (CSQ-8), a validated 8-item patient-reported outcome measure evaluating satisfaction with treatment, services received, and overall care experience. Total scores range from 8 to 32, with higher scores indicating greater satisfaction with treatment outcomes and care. Scale Information: Client Satisfaction Questionnaire (CSQ-8) Minimum Value: 8 Maximum Value: 32 Interpretation: Higher scores indicate greater patient satisfaction and better perceived treatment outcomes. |
Week 12 and Week 24
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Neuroma Maximum Diameter Measured by High-Resolution Ultrasound
Prazo: Baseline and Week 24
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Neuroma size will be assessed using high-resolution ultrasound. The maximum neuroma diameter will be measured in the longitudinal or transverse plane and recorded in millimeters (mm). The largest measured diameter will be used for analysis. Unit of Measure: Millimeters (mm) Minimum Value: 0 mm Maximum Value: No predefined maximum value Interpretation: Higher values indicate larger neuroma size and greater structural abnormality. |
Baseline and Week 24
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Colaboradores e Investigadores
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
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Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Dor
- Manifestações Neurológicas
- Doenças do Sistema Nervoso
- Complicações pós-operatórias
- Processos Patológicos
- Doenças Neuromusculares
- Doenças do Sistema Nervoso Periférico
- Manifestações Neurocomportamentais
- Distúrbios Perceptivos
- Dor, Pós-operatório
- Condições Patológicas, Sinais e Sintomas
- Sinais e sintomas
- Neuralgia
- Membro fantasma
- Aminoácidos, peptídeos e proteínas
- Proteínas
- Fatores biológicos
- Hidrolases
- Enzimas
- Enzimas e coenzimas
- Toxinas botulínicas
- Metaloendopeptidases
- Endopeptidases
- Hidrolases peptídicas
- Metaloproteases
- Proteínas bacterianas
- Toxinas bacterianas
- Toxinas, biológicas
- Toxinas Botulínicas, Tipo A
- incobotulinumtoxinaA
Outros números de identificação do estudo
- 2205v0123052026
- UARA-NEUROQUIET (Outro identificador: UARA-NEUROQUIET)
Plano para dados de participantes individuais (IPD)
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Descrição do plano IPD
Prazo de Compartilhamento de IPD
Critérios de acesso de compartilhamento IPD
Tipo de informação de suporte de compartilhamento de IPD
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