- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT01652053
A Pilot Study of the InterCushion Disc Nucleus Prosthesis (DNP) in Patients Receiving Discectomy
A Pilot Clinical Study to Assess the Safety and Effectiveness of the InterCushion Disc Nucleus Prosthesis in Patients Receiving Discectomy
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Tipo de estudo
Inscrição (Antecipado)
Contactos e Locais
Locais de estudo
-
-
Manitoba
-
Brandon, Manitoba, Canadá, R7A 2B3
- Recrutamento
- Brandon Regional Health Center
-
Contato:
- Jeff Felt, MD
- Número de telefone: 612-708-4838
- E-mail: jfelt@vti-spine.com
-
Contato:
- Ben A. Wasscher, MBA
- Número de telefone: 763-218-4311
- E-mail: bwasscher@vti-spine.com
-
Investigador principal:
- Phillip de Mueleneare, MD
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
Descrição
Inclusion Criteria:
- Patient has signed and dated a study specific informed consent form approved by the reviewing Institutional Review Board or Ethics Committee.
- Patient is 21 to 60 years of age.
- Patient is skeletally mature
- Patient requires a discectomy of one level from L2-S1.
- Patient has less than 50% loss of disc height at the affected level.
- Patient has persistent pain (predominantly leg pain, although some back pain that occurred at the same time as the leg pain and is believed to be associated with the disc herniation will not disqualify the patient from participating in this study) and symptoms despite a minimum of six weeks of non-operative treatment.
- Patient X-ray, CT or MR evidence of a herniated disc at the affected level.
- Patient has a minimum leg pain score of 6 cm on a 10 cm (i.e. 60 mm on a 100 mm) point visual analog scale (VAS).
- Patient has a minimum Oswestry Disability Index score of 40% (based upon a 100% scale).
- Patient is physically and mentally willing and able to comply with the postoperative scheduled clinical and radiographic evaluations and rehabilitation.
Exclusion Criteria:
- Patient has had any previous surgery at the affected levels.
- Patient has had any attempt at spinal fusion, at any lumbar levels.
- Patient has motion of < 3 degrees on pre-operative lateral flexion/extension radiographs
- Patient has a BMI
- Patient has severe osteoporosis of the spine.
- Patient has previously undergone chemotherapy, immunosuppressive therapy or radiation to the local area.
- Patient has active local or systemic infection.
- Patient has any known active malignancy.
- Patient has rheumatoid arthritis or systemic lupus erythematosus, or other chronic, inflammatory autoimmune disorder.
- Patient has ankylosing spondylitis or other spondyloarthropathy.
- Patient has spondylolisthesis.
- Patient is pregnant or plans to become pregnant during the course of the study.
- Patient has other concurrent physical or mental conditions that are likely to affect their outcome.
- Patient has congenital stenosis
- Patient is diabetic.
- The patient has osteoporosis or severe osteopenia as determined by the Investigator. Females over 40 with bone density score less than -1. A clinical SCORE calculator may also be utilized for females over 40 years of age.
- Patient has significant facet disease.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
Intervenção / Tratamento |
|---|---|
|
Disc Nucleus Replacement
Disc Nucleus Replacement (InterCushion DNP)
|
The device is intended for spinal arthroplasty in skeletally mature patients with leg pain due to a herniated disc with or without back pain, who are having a discectomy at one level from L2 -S1.
These patients should have no spondylolisthesis at the involved level.
Outros nomes:
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Decrease in ODI
Prazo: 6 months
|
Improvement in the Oswestry Disability Index (ODI) score i.e. decrease of 15% or better ODI.
|
6 months
|
|
Decrease in VAS
Prazo: 6 months
|
Improvement in leg pain evidenced by decrease in pain score of at least 2 cm (i.e.
20 mm) on the visual analog scale (VAS)
|
6 months
|
|
Maintenance of post-operative disc height
Prazo: 6 months
|
Disc at the treated level is collapsed by ≤ 15% when compared to an adjacent health level.
|
6 months
|
|
Mobility of treated segment
Prazo: 6 months
|
Motion of ≥ 3 degrees on lateral flexion/extension radiographs
|
6 months
|
|
Neurologic deficits
Prazo: 6 months
|
No new permanent neurological deficit or worsening of an existing permanent neurological deficit
|
6 months
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Maintenance or decrease in ODI
Prazo: 12 and 24 months
|
Maintenance of improvement or further improvement in the Oswestry Disability Index (ODI) score measured at six months i.e. decrease of 15% or better ODI.
|
12 and 24 months
|
|
Maintenance or decrease in VAS
Prazo: 12 and 24 months
|
Maintenance of improvement or further improvement in leg pain evidenced by decrease in pain score on the visual analog scale (VAS)
|
12 and 24 months
|
|
Maintenance of post-operative disc height.
Prazo: 12 and 24 months
|
Disc at the treated level is collapsed by ≤ 15% when compared to an adjacent health level.
|
12 and 24 months
|
|
Mobility of treated segment
Prazo: 12 and 24 months
|
Motion of ≥ 3 degrees on lateral flexion/extension radiographs
|
12 and 24 months
|
|
Neurological deficits
Prazo: 12 and 24 months
|
No new permanent neurological deficit or worsening of an existing permanent neurological deficit
|
12 and 24 months
|
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Failures
Prazo: 6, 12 and 24 months
|
Revision: is a procedure that adjusts or in any way modifies or removes part of the original implant configuration, with or without replacement of a component. Removal: is a procedure where the entire original system configuration is removed with or without replacement. Supplemental fixation: a procedure in which additional instrumentation not under study is implanted. |
6, 12 and 24 months
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Phillip F de Muelanaere, MD, Brandon General Hospital
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Antecipado)
Conclusão do estudo (Antecipado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- CP 2010-001
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
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