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NEUROCUPLE™ en pacientes con ATR

22 de octubre de 2026 actualizado por: nCap Medical

Mejora del tratamiento del dolor en pacientes con reemplazo de rodilla mediante un innovador dispositivo no invasivo y ahorrador de opioides (NEUROCUPLE™)

This is a randomized (1:1) placebo-controlled clinical trial to determine the feasibility and effectiveness of 30-day application of NEUROCUPLE™ patch for pain reduction and opioid consumption following TKA. Results will establish NEUROCUPLE™ as an effective non-opioid postoperative pain management device for FDA approval. Importantly, we have a placebo device (device without the captor array layer) that looks exactly like the active device, allowing us to conduct a true placebo randomized study.

Descripción general del estudio

Descripción detallada

Total knee arthroplasty (TKA) is the most common elective surgical procedure. By 2030, 3.5 million TKA procedures are expected1 to be performed. Multiple factors can contribute to an individual's need for TKA; however, the primary factor is osteoarthritis15 and pain. Osteoarthritis affects approximately 32.5 million individuals in the US, leading to an enormous economic burden, ranging from $15-$16 billion dollars annually. Although most diagnosed with osteoarthritis should undergo TKA, the fear of experiencing severe long lasting postoperative pain causes many to postpone the surgery. For those that do elect surgery, postoperative pain decreases quality of life and an increase in risk of chronic opioid use. Out of 98,623 individuals who received TKA from 2015 to 2019, it was reported that 72% received opioid prescriptions in duration and dosage, which was proposed to be the cause of long-term opioid use.

Postoperative pain strategies for TKA often requires opioid use. To mitigate postoperative pain management following TKA a multimodal approach is often used as a part of enhanced recovery after surgery (ERAS) protocols. This approach on the use of on peripheral nerve blocks (PNB)s, acetaminophen, non-steroidal anti-inflammatory drugs (NSAIDs), and opioids13,18,19. Postoperative opioid and NSAIDS can lead to excessive sedation, vomiting, nausea, hypotension, major bleeding, life-threatening respiratory depression, constipation, renal failure, frequent delayed functional recovery, increase cost of care, and prolong hospital stay. Furthermore, the postoperative prescription of use opioids leads to long-term opioid users in 34.7% to 53.5%. Patients with poorly controlled acute surgical pain are at risk for chronic post-surgical pain, opioid dependence, and long-term opioid use. Thus, there is an urgent and unmet clinical need for a reliable technology to predict and reduce opioid use and costly opioid adverse effects while enhancing surgical pain relief. On an economic point of view, evidence also demonstrates that persistent postoperative pain leads to a loss in work productivity and absenteeism, mounting to an average loss of $13,761 per individual. Therefore, there is a significant need for alternative non-pharmacological, and non-opioid therapies that are effective in treating postoperative pain management in patients undergoing TKA.

Clinical approaches associated with postoperative pain and opioids in TKA. Data compiled from 90 million patients from 38 hospital networks and 18 non-network hospitals demonstrated that reliance on opioids for postoperative pain management is still extremely high (91.5%) following a TKA. Evidence supporting the use of PNBs is lacking and their use may increase the risk of fall. Sharma et al., 2010 reported that femoral nerve blocks conducted in 709 patients lead to postoperative falls (n=13 patients). A study including 250 patients demonstrated that postoperative falls led to an extended hospital stay. Furthermore, nerve injury and major bleeding have also been reported following PNBs. Complementary techniques such as Transcutaneous Electrical Nerve Stimulation (TENS), acupuncture and hypnosis have been proposed but evidence supporting the use of these techniques is still limited and the use of these techniques requires expertise and time. Therefore, current postoperative pain treatments remain unsatisfactory.

A pain relief patch that provides a clinically effective alternative to opioid use for pain management. The scientific premise of our proposal rests upon the published literature and our preliminary data that demonstrates the use of pain relief patches for pain management. Pain and local inflammation following tissue injuries is the result of the release of a number of mediators and ions, decreases in pH (increase in acidity), and changes in local electrical potential. This is in part due to the central nervous system stimulation of nociceptors and the anterior and lateral spinothalamic tracts. The NEUROCUPLE™ device's millions of nanocapacitors capture and release the excess electrical load generated by trauma, thus blocking the transmission of the local pain signals.

An observational study evaluating non-surgical patients' (n=66) using our licensed nanotechnology topical analgesic demonstrated a 71% reduction in Brief Pain Inventory pain severity (Fig. 1), improvements in quality of life, and a 98% reduction in oral pain medication use. Our additional preliminary data in patients undergoing a TKA demonstrated that the use of the patch device plus standard on care was associated with a 36% reduction in pain at rest by postoperative day 3 and more importantly a reduction of 47% in the number of patients requesting an opioid refill beyond their initial prescription within the first 30 days compared to the patients receiving only standard of care. Thus, we believe our clinical data provides a strong scientific premise for utilizing pain relief patches as an alternative to analgesic drugs to provide effective and safe postoperative approach to reduce postoperative analgesia and more importantly to greatly reduce the number of patients requiring long term opioid exposure which has been demonstrated as a risk for postoperative opioid use disorder (OUD) in surgical patients.

Tipo de estudio

Intervencionista

Inscripción (Actual)

156

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Pennsylvania
      • Pittsburgh, Pennsylvania, Estados Unidos, 15232
        • UPMC Shadyside Hospital

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • >18 years of age
  • Scheduled for elective primary unilateral TKA
  • T-score < 60 on the PROMIS Anxiety measure

Exclusion Criteria:

  • Children (<18 yr.)
  • Pregnant women
  • Active alcoholism (defined as daily use of more than 1 liter of wine and /or 3 or more shots of hard liquor) or drug abuse (defined as daily use of illicit drugs)
  • Severe chronic pain condition that requires daily preoperative opioid dependence
  • T-score ≥ 60 in any of the three PROMIS measures (i.e., sleep, anxiety, and depression)
  • Other concomitant surgery being performed in addition to TKA
  • Patients undergoing bilateral TKA
  • Patients undergoing knee replacement revision
  • Patients with limited mobility (in a wheelchair or requiring a walker)
  • Patients who are not returning home after surgery

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: NEUROCUPLE™ Group

This arm of subjects will receive the active NEUROCUPLE™ patch to wear for 2-weeks following their TKA surgery.

nCAP Medical has developed an effective, safe, non-opioid alternative, the NEUROCUPLE™ device, based on an innovative nanotechnology to reduce surgical pain and facilitate functional recovery while reducing opioid prescriptions, opioid-related adverse events and reducing the cost of care in millions of Americans undergoing TKA each year.

Comparador de placebos: Placebo Group

This arm of subjects will receive the placebo (non-active, sham) patch to wear for 2-weeks following their TKA surgery.

The placebo patch is identical to the active patch but with no active agents.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Post-operative Pain at Rest
Periodo de tiempo: 1-Week Post Hospital Discharge

Pain at rest will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

1-Week Post Hospital Discharge

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of Participants With Post-Operative Nausea and Vomiting (PONV) and Antiemetic Use
Periodo de tiempo: Up to 24-hours post-operatively

Incidence of PONV measured by antiemetic use yes/no

Up to 24-hours post-operatively
Time to Hospital Discharge (Length of Hospital Stay)
Periodo de tiempo: Up to post-operative day 10

The length of the hospital stay will be abstracted from the medical records, and the mean time and full range will be reported in hours

Up to post-operative day 10
Total Opioid Use in OME (mg) (in Hospital)
Periodo de tiempo: Up to 24-hours post-operatively

OME measured in mg

Up to 24-hours post-operatively
Total Opioid Use in OME (mg) at 1 Week Post-Hospital Discharge
Periodo de tiempo: One-week Post Hospital Discharge

OME measured in mg

One-week Post Hospital Discharge
Post-Operative Pain Scores (NRS)
Periodo de tiempo: Up to 24-hours post-operatively

Assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

Up to 24-hours post-operatively

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Baseline Pain at Rest
Periodo de tiempo: Prior to day of surgery

Pain at rest will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

Prior to day of surgery
Pain While Walking 30 Feet, Baseline
Periodo de tiempo: Prior to day of surgery

Pain while walking 30 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

Prior to day of surgery
Pain While Walking 30 Feet, 1-week Post-op
Periodo de tiempo: 1-Week Post Hospital Discharge

Pain while walking 30 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

1-Week Post Hospital Discharge
Pain While Walking 30 Feet, 6-weeks Post-op
Periodo de tiempo: 6-Weeks Post Hospital Discharge

Pain while walking 30 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

6-Weeks Post Hospital Discharge
Pain While Walking 100 Feet, Baseline
Periodo de tiempo: Prior to day of surgery

Pain while walking 100 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

Prior to day of surgery
Pain While Walking 30 Feet, 2-weeks Post-op
Periodo de tiempo: 2-Weeks Post Hospital Discharge

Pain while walking 30 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

2-Weeks Post Hospital Discharge
Pain While Walking 100 Feet, 1-week Post-op
Periodo de tiempo: 1-Week Post Hospital Discharge

Pain while walking 100 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

1-Week Post Hospital Discharge
Pain While Walking 100 Feet, 2-weeks Post-op
Periodo de tiempo: 2-Weeks Post Hospital Discharge

Pain while walking 100 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

2-Weeks Post Hospital Discharge
Pain While Walking 100 Feet, 6-weeks Post-op
Periodo de tiempo: 6-Weeks Post Hospital Discharge

Pain while walking 100 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

6-Weeks Post Hospital Discharge
Opioid Prescriptions Within the First 6-weeks Following Surgery
Periodo de tiempo: 6-Weeks Post Hospital Discharge

The number of opioid refills will be collected via Prescription Drug Monitoring Program (PDMP) for up to 6-weeks following hospital discharge. This will be averaged across each group and reported as a Mean(SD).

6-Weeks Post Hospital Discharge
Patient Satisfaction With Overall Care
Periodo de tiempo: 2-Weeks and 6-Weeks Post Hospital Discharge

Scale from 0 (least satisfied) to 10 (most satisfied)

2-Weeks and 6-Weeks Post Hospital Discharge
Patient Satisfaction With Pain Management
Periodo de tiempo: 2-Weeks and 6-Weeks Post Hospital Discharge

Scale from 0 (least satisfied) to 10 (most satisfied)

2-Weeks and 6-Weeks Post Hospital Discharge
Pain While Walking 100 Feet, 24-hours Post-op
Periodo de tiempo: 24-hours post-operatively

Pain while walking 100 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

24-hours post-operatively
Pain While Walking 30 Feet, 24-hours Post-op
Periodo de tiempo: 24-hours post-operatively

Pain while walking 30 feet will be assessed by a numerical rate scale (NRS), in which 0 = no pain at all and 10 = the worst pain imaginable

24-hours post-operatively

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Jacques E. Chelly, MD, PhD, MBA, University of Pittsburgh / UPMC

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

25 de septiembre de 2024

Finalización primaria (Actual)

18 de julio de 2025

Finalización del estudio (Actual)

18 de julio de 2025

Fechas de registro del estudio

Enviado por primera vez

11 de junio de 2024

Primero enviado que cumplió con los criterios de control de calidad

11 de junio de 2024

Publicado por primera vez (Actual)

14 de junio de 2024

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

22 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

Sí

producto fabricado y exportado desde los EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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