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RetiradoNCT07213843Registro de ClinicalTrials.gov

Combined Circulatory and Dietary Interventions for Neuropathy

Diabete Type 2 · Neuropathy, Painful

LO ESENCIAL

De qué trata este estudio

El registro no identifica actualmente este estudio como reclutando. Consulta su estado antes de planificar una evaluación.

Tipo de estudio
De intervención
Fase
No aplica
Rango de edad
35 años - 85 años
Sexo admitido
Todos los sexos
Voluntarios sanos
No aceptados
Participantes
0 Real

Estos son puntos de partida, no una decisión de elegibilidad. El equipo debe revisar todos los requisitos.

Por qué se detuvo el estudio

Study was never initiated/no study participants were ever enrolled/study was never funded.

Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.

Acerca de la investigación

The purpose of this study is to evaluate the effectiveness of three different interventions in improving neuropathy symptoms in individuals aged 35-85 with moderate to severe neuropathy. The study will compare three treatment groups: Intraneural Facilitation® (INF®) therapy alone, INF® therapy combined with Neuro vascular index (NVI) food-guided elimination (NVIf), and NVIf alone. The aim is to determine which treatment results in the greatest improvement in neuropathy symptoms, including quality of life, sensory and pain improvements, and functional outcomes.

Leer la descripción completa

The purpose of this investigator-initiated study is to observe the effectiveness of a manual physical therapy technique known as Intraneural Facilitation (INF®), both independently and in combination with a Nutritional Vascular Inflammation focused (NVIf) dietary intervention, in improving neurovascular function, pain, and physical performance in individuals with moderate to severe peripheral neuropathy (PN). Subjects will be randomized into one of the three interventions arms: (1) INF® therapy alone, (2) NVIf intervention alone or (3) a combination of both. INF® is a manual therapy, while NVIf utilizes ultrasound guided food elimination. Outcomes include pain (Visual analog scale), sensory function (Semmes Weinstein Monofilament), physical function (Lower extremity functional scale, 10-meter walk test, timed up and go) quality of life (Norfolk Quality of life-Diabetic neuropathy), and neurovascular blood flow analysis. Study participants will be 35-85 years old with a physician-confirmed diagnosis of moderate to severe lower extremity peripheral neuropathy and at least one symptom: numbness, tingling, burning, sharp pain, or increased sensitivity. They must score 0-60 on the Lower Extremity Functional Scale (LEFS), speak and understand English, provide written informed consent, and be willing to complete all study procedures, including intervention and follow-up visits. Participants must be able to ambulate independently with or without an assistive device. Subjects will be recruited using email and flyer through the Neuropathic Therapy Center (NTC) research interest list and through providers at Loma Linda's University (LLU) Health offices. 60 subjects will be recruited, and consent will take place at the LLU or at the Murrieta study site prior to randomization, administered by trained study staff authorized to obtain informed consent.

¿Quién podría participar?

La lista siguiente contiene el texto del patrocinador. Puede incluir condiciones, tratamientos previos, resultados de pruebas y otros requisitos. Aparecer en tu búsqueda no significa que califiques.

Inclusion Criteria

  • Confirmed diagnosis of peripheral neuropathy in the lower extremities by a physician
  • Lower Extremity Functional Scale (LEFS) score between 0-60 (indicating moderate to significant difficulty in lower extremity function)
  • Ability to speak and understand English
  • Ability to provide appropriate written informed consent
  • Willingness to participate in all study procedures, including the intervention and follow-up visits
  • Ability to ambulate independently with or without an assistive device

Exclusion Criteria

  • Any medical condition suggesting potential decline in function over the next 6 months (e.g., ongoing chemotherapy, radiation therapy, or dialysis)
  • Active alcohol or drug misuse
  • End-stage renal failure
  • Uncontrolled hypertension
  • Severe dyslipidemia
  • Chronic liver disease
  • Autoimmune disease
  • Advanced chronic obstructive pulmonary disease (COPD)
  • Active inflammation
  • Shingles-related neuropathy
  • Presence of any lower extremity amputations or significant wounds
  • Severe chronic medical conditions requiring active treatment that could interfere with study outcomes
  • Morbid obesity
  • Concomitant use of medications or devices that may interfere with study results or are not allowed per protocol
  • Inability to comprehend or provide informed consent
  • Inability to speak or understand English
  • Pregnancy, breastfeeding, or planning pregnancy during the study period (female participants)
  • Inability or unwillingness to adhere to study procedures, including dietary guidelines or follow-up visits
  • Inability to complete all required study assessments, including follow-up appointments and questionnaires
Entiende la evaluación inicial

Tratamiento, grupos y participación

El registro puede describir tratamientos y duración sin incluir un calendario completo. Pide al equipo las visitas, procedimientos, riesgos, costos y alternativas. Mantén tu atención habitual salvo que tu médico te indique un cambio.

Asignación
Asignación al azar
Enmascaramiento
Sin enmascaramiento
INF® Therapy Only Group

INF® therapy is a manual technique designed to improve neural circulation by using a series of manual holds administered by a trained practitioner. Participants will receive 60-minute sessions, 2-3 times per week, for a total of 8 sessions.

Other: INF® Therapy

NVIf Only Group

NVIf, is a dietary intervention that uses a patented ultrasound technology to assess vascular responses to food allergens. By identifying foods that exacerbate inflammation and restrict circulation, the intervention guides patients to eliminate these foods, thereby improving nerve health. Those in this group will participate in follow-up for food elimination adherence, including daily tracking of foods ingested. Week 1-2: 4 x NVI food guided-elimination visits. Week 2-5 complete weekly Likert scale inquiring about food eliminations and weekly phone call check-in attempts will be made by research staff.

Other: NVIf

INF® Therapy + NVIf Group

INF® therapy and NVI Food-Guided Elimination Group: Week 1-2: 4 x NVI food guided-elimination visits. Participants will receive 60-minute sessions, 2-3 times per week, for a total of 8 sessions. As well as participate in NVIf, which is a dietary intervention that uses a patented ultrasound technology to assess vascular responses to food allergens. By identifying foods that exacerbate inflammation and restrict circulation, the intervention guides patients to eliminate these foods, thereby improving nerve health. Those in this group will participate in follow-up for food elimination adherence, including daily tracking of foods ingested. Week 2-5 complete weekly Likert scale inquiring about food eliminations and weekly phone call check-in attempts will be made by research staff as well as INF® therapy for 60-minute sessions, 2-3 times per week, for a total of 8 sessions.

Other: INF® Therapy · Other: NVIf

INF® Therapy OTHER

INF® therapy is a manual technique designed to improve neural circulation by using a series of manual holds administered by a trained practitioner,

NVIf OTHER

NVIf is a dietary intervention that uses a patented ultrasound technology to assess vascular responses to food allergens

Prepara tus preguntas

Qué evalúan los investigadores

Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.

Medidas principales

Change in Pain Intensity

Plazo: Baseline (Week 0) and post-intervention (Week 4-5)

Pain intensity will be assessed using the Visual Analog Scale. Improvement will be indicated by reduced VAS scores. Unit of Measure: Millimeters on a 0-100 mm scale.

Change in Sensory Function

Plazo: Baseline (Week 0), mid-treatment (Week 3), and post-intervention (Week 4-5)

Sensory function will be assessed using the Semmes-Weinstein Monofilament test. Improvement will be indicated by increased monofilament detection. Detection threshold in grams (monofilament response: detected/not detected)

Change in Functional Limitation

Plazo: Baseline (Week 0) and post-intervention (Week 4-5)

Functional limitation related to neuropathy will be assessed using the Lower Extremity Functional Scale. Improvement will be indicated by higher Lower Extremity Functional Scale scores. Scale score (0-80).

Change in Gait Speed

Plazo: Baseline (Week 0), mid-treatment (Week 3), and post-intervention (Week 4-5)

Gait speed will be assessed using the 10-Meter Walk Test. Improvement will be indicated by faster walk time. Seconds to complete 10 meters (converted to meters/second if applicable)

Change in Mobility and Fall Risk

Plazo: Baseline (Week 0), mid-treatment (Week 3), and post-intervention (Week 4-5)

Mobility and fall risk will be assessed using the Timed Up and Go (TUG) test. Improvement will be indicated by shorter completion times. Unit of Measure: Seconds.

Medidas secundarias

Change in Quality of Life

Plazo: Baseline (Week 0) and post-intervention (Week 4-5)

Quality of life will be measured using the Norfolk Quality of Life-Diabetic Neuropathy questionnaire to determine the effect of each treatment approach on overall patient well-being. Higher scores indicate greater impairment; a reduction reflects improved quality of life. Lowest score=0, means best quality of life with little to no neuropathy impacts. A maximum score of 138, means worst quality of life with severe impairments.

Otras medidas

Change in Neurovascular Function and Inflammation

Plazo: Baseline (Week 0) and post-intervention (Week 4-5)

Mechanistic analysis will be performed using the Neurovascular Index with Philips Affinity 50 Ultrasound to evaluate changes in microvascular resistance and neurovascular blood flow, as well as the effect of NVI-guided food elimination on reducing neurovascular inflammation.

El registro no indica resultados publicados.

Revisa las tablas completas y sus limitaciones en el registro oficial.

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Centros de investigación (1)

El estado general puede diferir del estado de un centro. Confirma la disponibilidad antes de trasladarte.

1 centros

Neuropathic Therapy CenterLoma Linda, California, United StatesEstado desconocido

Equipo y fechas

Patrocinador principal
Loma Linda University
Inicio del estudio
1 oct 2026 Estimado
Finalización primaria
1 oct 2028 Estimado
Finalización del estudio
1 dic 2028 Estimado
Primera publicación
9 oct 2025 Real
Última actualización
10 nov 2026 Real

Contactos oficiales del estudio

No hay un contacto central indicado. Revisa los centros y el registro oficial.

Título oficial del estudio

Combined Circulatory and Dietary Interventions for Neuropathy (CDIN)

EL PRÓXIMO PASO, CON APOYO HUMANO

Consulta a Wellness Clinical Research

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Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.

Consultado: 12 nov 2026 · Última actualización del registro: 10 nov 2026