- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiesteder
-
-
Manitoba
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Brandon, Manitoba, Canada, R7A 2B3
- Rekruttering
- Brandon Regional Health Center
-
Kontakt:
- Jeff Felt, MD
- Telefonnummer: 612-708-4838
- E-mail: jfelt@vti-spine.com
-
Kontakt:
- Ben A. Wasscher, MBA
- Telefonnummer: 763-218-4311
- E-mail: bwasscher@vti-spine.com
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Ledende efterforsker:
- Phillip de Mueleneare, MD
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
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.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Decrease in ODI
Tidsramme: 6 months
|
Improvement in the Oswestry Disability Index (ODI) score i.e. decrease of 15% or better ODI.
|
6 months
|
|
Decrease in VAS
Tidsramme: 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
Tidsramme: 6 months
|
Disc at the treated level is collapsed by ≤ 15% when compared to an adjacent health level.
|
6 months
|
|
Mobility of treated segment
Tidsramme: 6 months
|
Motion of ≥ 3 degrees on lateral flexion/extension radiographs
|
6 months
|
|
Neurologic deficits
Tidsramme: 6 months
|
No new permanent neurological deficit or worsening of an existing permanent neurological deficit
|
6 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Maintenance or decrease in ODI
Tidsramme: 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
Tidsramme: 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.
Tidsramme: 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
Tidsramme: 12 and 24 months
|
Motion of ≥ 3 degrees on lateral flexion/extension radiographs
|
12 and 24 months
|
|
Neurological deficits
Tidsramme: 12 and 24 months
|
No new permanent neurological deficit or worsening of an existing permanent neurological deficit
|
12 and 24 months
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Failures
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Phillip F de Muelanaere, MD, Brandon General Hospital
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CP 2010-001
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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-
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-
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Synthes USA HQ, Inc.AfsluttetDegenerativ diskussygdomForenede Stater
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Spinal Stabilization TechnologiesAfsluttetKroniske lændesmerter | Degenerativ diskussygdomParaguay
-
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