- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07681921
Randomized Clinical Investigation of Photobiomodulation (PBM) for the Management of Early Peripheral Neuropathy Related to Medical Oncologic Therapy (ENL)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Chemotherapy-induced peripheral neuropathy (PN) is a common side-effect of many anti-neoplastic agents; its prevalence is estimated to 20-50% but varies considerably according to many factors and might actually be underreported. PN is increasingly reported as a complication of cancer immunotherapy and various targeted therapies currently used for the treatment of cancer.
PN typically causes disabling, sensitive (paresthesia, dysesthesia, allodynia, loss of sensation), but can also cause motor dysfunction (muscle weakness, fatigue) and autonomic dysfunction (digestive disorders, orthostatic hypotension); once established, regression of symptoms is slow. The pathobiology of chemotherapy-induced PN is mainly unknown despite the documented involvement of neuroinflammatory, mitochondrial, and vascular mechanisms.
PN often compromises quality of life and is a frequent reason for dose reduction, treatment delay, or premature discontinuation of anticancer therapy.
So far, no standard therapy has been recommended, with the possible exception of duloxetine, which has been associated with a modest symptom improvement in cisplatin-treated patients.
In this context, innovative, non-pharmacological, and well-tolerated strategies are needed. Photobiomodulation (PBM), also known as low-level laser therapy (LLLT), uses specific wavelengths (red or near-infrared) to modulate cellular activity, promote nerve regeneration, reduce inflammation, and regulate pain. Already included in international recommendations for the management of oral mucositis induced by chemotherapy or radiotherapy, PBM is emerging as a potentially effective alternative for other cancer-related toxicities.
A beneficial effect of PBM on diabetic PN and oxaliplatin-induced PN has been reported.
Argenta et al. published a small randomized sham-controlled trial of PBM on chemotherapy-induced PN that indicated a significant reduction in neuropathy symptoms. They found a significant benefit already after 4 weeks of therapy and patients who crossed over from sham laser experienced similar benefits. In a pilot trial, Lodewijckx et al. found a considerable decrease in symptoms of chemotherapy-induced PN with PBM. The same group reported " promising " results with PBM for the prevention of chemotherapy-induced PN in breast cancer patients.
Therefore, the investigator plan to evaluate the role of PBM administered to patients with " de novo " early signs of PN that are supposed to be related to ongoing neurotoxic anti-cancer therapy (Bortezomib, Cisplatin, Docetaxel, Enfortumag, Halaven, Oxaliplatin, Paclitaxel, Vinblastine, Vincritsine, Vinorelbine).
The project is therefore part of a proactive approach to supportive care aimed at reducing the early symptoms of PN, improving patients' quality of life, and avoiding the interruption or reduction of cancer therapy doses, using a simple, non-invasive device that has the potential for widespread application.
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Brabant
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Brussels, Brabant, Bélgica, 1070
- Jules Bordet Institute
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- All the patients admitted for medical oncological therapy to the day care facility (Hôpital de Jour) are eligible for the protocol.
- Age 18 years or above
- Have no documented or observable psychiatric or neurological disorders that might interfere with study participation (e.g., dementia or psychosis)
- Be able to understand the ICF and study-related questionnaires
- Signed informed consent
Exclusion Criteria:
- severe or unstable cardio-respiratory or musculoskeletal disease
- Peripheral neuropathy previous to chemotherapy
- Receiving potentially neurotoxic therapies other than given for cancer treatment
- Interruption of more than two consecutive laser treatments
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Cuidados de apoyo
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: PBM group
Patient will recieve photobiomodulation of 20J/cm2 twice a week.
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Patients will receive 20 Joule/cm2
Otros nombres:
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Comparador falso: Sham-PBM group
Patient will recieve a simulated treatment by photobiomodulation twice a week.
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Patients will receive 20 Joule/cm2
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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severity of CIPN measured by modified Total Neurpathy Score m-TNS
Periodo de tiempo: At baseline (week 0) and at week 3 and week 6
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Include several simple neurological tests
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At baseline (week 0) and at week 3 and week 6
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Pain & satisfaction by Numeric Rating Scale (0-10)
Periodo de tiempo: At baseline (Week0), and Week 3 and Week 6
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Pain & satisfaction by Numeric Rating Scale (0-10)
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At baseline (Week0), and Week 3 and Week 6
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Mobility by 6min walking test
Periodo de tiempo: At baseline (Week0), and Week 3 and Week 6
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Mobility by 6min walking test and
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At baseline (Week0), and Week 3 and Week 6
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Quality of life by FACT-GOG-NTX questionnair
Periodo de tiempo: At baseline (Week0), and Week 3 and Week 6
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Quality of life by FACT-GOG-NTX questionnaire
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At baseline (Week0), and Week 3 and Week 6
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- IJB-EARLYNEUROLASER-2026
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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