- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT06460350
NEUROCUPLE™ en pacientes con ATR
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
Estado
Condiciones
Intervención / Tratamiento
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
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Pennsylvania
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Pittsburgh, Pennsylvania, Estados Unidos, 15232
- UPMC Shadyside Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
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
¿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
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Jacques E. Chelly, MD, PhD, MBA, University of Pittsburgh / UPMC
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
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
- STUDY24020075
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.
producto fabricado y exportado desde los EE. UU.
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