- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Anticipato)
Contatti e Sedi
Luoghi di studio
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Manitoba
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Brandon, Manitoba, Canada, R7A 2B3
- Reclutamento
- Brandon Regional Health Center
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Contatto:
- Jeff Felt, MD
- Numero di telefono: 612-708-4838
- Email: jfelt@vti-spine.com
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Contatto:
- Ben A. Wasscher, MBA
- Numero di telefono: 763-218-4311
- Email: bwasscher@vti-spine.com
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Investigatore principale:
- Phillip de Mueleneare, MD
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Metodo di campionamento
Popolazione di studio
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
|---|---|
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Disc Nucleus Replacement
Disc Nucleus Replacement (InterCushion DNP)
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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.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Decrease in ODI
Lasso di tempo: 6 months
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Improvement in the Oswestry Disability Index (ODI) score i.e. decrease of 15% or better ODI.
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6 months
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Decrease in VAS
Lasso di tempo: 6 months
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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)
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6 months
|
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Maintenance of post-operative disc height
Lasso di tempo: 6 months
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Disc at the treated level is collapsed by ≤ 15% when compared to an adjacent health level.
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6 months
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Mobility of treated segment
Lasso di tempo: 6 months
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Motion of ≥ 3 degrees on lateral flexion/extension radiographs
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6 months
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Neurologic deficits
Lasso di tempo: 6 months
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No new permanent neurological deficit or worsening of an existing permanent neurological deficit
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6 months
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Maintenance or decrease in ODI
Lasso di tempo: 12 and 24 months
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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.
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12 and 24 months
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Maintenance or decrease in VAS
Lasso di tempo: 12 and 24 months
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Maintenance of improvement or further improvement in leg pain evidenced by decrease in pain score on the visual analog scale (VAS)
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12 and 24 months
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Maintenance of post-operative disc height.
Lasso di tempo: 12 and 24 months
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Disc at the treated level is collapsed by ≤ 15% when compared to an adjacent health level.
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12 and 24 months
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Mobility of treated segment
Lasso di tempo: 12 and 24 months
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Motion of ≥ 3 degrees on lateral flexion/extension radiographs
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12 and 24 months
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Neurological deficits
Lasso di tempo: 12 and 24 months
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No new permanent neurological deficit or worsening of an existing permanent neurological deficit
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12 and 24 months
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Failures
Lasso di tempo: 6, 12 and 24 months
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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
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Phillip F de Muelanaere, MD, Brandon General Hospital
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Anticipato)
Completamento dello studio (Anticipato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- CP 2010-001
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Disc Nucleus Replacement (InterCushion DNP)
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VIVEX Biologics, Inc.Attivo, non reclutanteLombalgia | Malattia degenerativa del disco | Degenerazione del discoStati Uniti
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VIVEX Biologics, Inc.MCRAAttivo, non reclutanteLombalgia | Malattia degenerativa del disco | Degenerazione del discoStati Uniti
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VIVEX Biologics, Inc.ReclutamentoMalattia degenerativa del disco | Degenerazione del disco | Dolore discogenico lombareStati Uniti