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
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
상세 설명
연구 유형
연구 유형
등록 (예상)
등록
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Laurie E Lynch, PhD
- 전화번호: 952-221-2468
- 이메일: laurie.lynch@visi.com
연구 연락처 백업
- 이름: Felt Jeff, MD
- 전화번호: 612-708-4838
- 이메일: jfelt@vti-spine.com
연구 장소
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Manitoba
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Brandon, Manitoba, 캐나다, R7A 2B3
- 모병
- Brandon Regional Health Center
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연락하다:
- Jeff Felt, MD
- 전화번호: 612-708-4838
- 이메일: jfelt@vti-spine.com
-
연락하다:
- Ben A. Wasscher, MBA
- 전화번호: 763-218-4311
- 이메일: bwasscher@vti-spine.com
-
수석 연구원:
- Phillip de Mueleneare, MD
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
설명
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.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
그룹/코호트 수
코호트 및 개입
그룹/코호트그룹/코호트 |
개입 / 치료개입 / 치료 |
|---|---|
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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.
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Decrease in ODI
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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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2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Maintenance or decrease in ODI
기간: 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
기간: 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.
기간: 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
기간: 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
기간: 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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기타 결과 측정
기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Failures
기간: 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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공동 작업자 및 조사자
수사관
수사관
- 수석 연구원: Phillip F de Muelanaere, MD, Brandon General Hospital
연구 기록 날짜
연구 주요 날짜
연구 시작
연구 시작
기본 완료 (예상)
기본 완료
연구 완료 (예상)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
기타 연구 ID 번호
기타 연구 ID 번호
- CP 2010-001
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .