Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion (APPRAISET1)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01013389
Recruitment Status : Completed
First Posted : November 13, 2009
Last Update Posted : April 5, 2017
Apatech, Inc.
Information provided by (Responsible Party):
Baxter Healthcare Corporation

November 10, 2009
November 13, 2009
April 5, 2017
June 2007
December 2012   (Final data collection date for primary outcome measure)
Fusion, defined as evidence of bridging trabecular bone present at 1 year as assessed by CT scan as well as a determination of no motion as assessed by plain radiographs. [ Time Frame: 1 year ]
Same as current
Complete list of historical versions of study NCT01013389 on Archive Site
Improvement clinical outcomes measurements compared to pre-opscores: pain/Disability as measured by Oswestry Lower Back Pain Questionnaire, quality of Life as measured by Short Form Health Survey (SF36), and neurological status [ Time Frame: 1 year ]
Same as current
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Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion
A Prospective, Randomised Study Comparing the Use of Actifuse (Trademark)ABX Synthetic Bone Substitute With INFUSE (Registrered Trademark) in Patients Requiring Posterolateral Instrumented Lumbar Fusion With Interbody Fusion

The primary objective of this clinical trial is to evaluate the success rates of Actifuse ABX and INFUSE in achieving bone fusion.

The secondary objective of this clinical trial is to assess clinical outcome measurements.

Not Provided
Not Applicable
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Degenerative Disc Disease
  • Procedure: Actifuse ABX
    bone substitute used for posterolateral instrumented lumbar fusion with interbody fusion
  • Procedure: INFUSE, plus master granules (MGG)
    bone substitute in posterolateral instrumented lumbar fusion with interbody fusion
  • Experimental: Actifuse ABX
    Actifuse ABX bone substitute
    Intervention: Procedure: Actifuse ABX
  • Active Comparator: INFUSE, plus master granules (MGG)
    synthetic bone substitute used in posterolateral instrumented lumber fusion with interbody fusion
    Intervention: Procedure: INFUSE, plus master granules (MGG)
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
December 2012
December 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Has degenerative disc disease of the lumbar spine as indicated by back pain of discogenic/degenerative origin, with or without leg pain, and has one or more of the following conditions as documented by plain X-rays, CT scan or MRI scan:

    • Modic changes.
    • High intensity changes in the annulus.
    • Loss of disc height.
    • Decreased hydration of the disc.
    • Canal stenosis with or without spondylotic slip.
    • Gross facet joint changes requiring fusion for treatment.
    • Have documented annular pathology by other means. (e.g., with discography).
  • Has a preoperative Oswestry Back Disability Score of 30 or more.
  • Aged 18 to 75 years and skeletally mature at time of surgery.
  • Has not responded to non-operative treatment (e.g., bed rest, physical therapy, medications and/or spinal injections) for a period of six months.
  • If of childbearing potential, patient is non-pregnant, non-nursing and agrees not to become pregnant for one year following surgery.
  • Is willing to and able to comply with the study plan and able to understand and sign the Patient Informed Consent Form.

Exclusion Criteria:

  • Has had previous failed attempts at fusion surgery at the involved level(s).
  • Has a diagnosis of spinal infection tumour or trauma.
  • Requires surgery at more than two (2) levels.
  • Has osteoporosis (excluding osteopenia) as evidenced on plain X-rays, CT scans (or DEXA scan in cases of doubt).
  • Is pregnant.
  • Is an alcohol and/or drug abuser as defined by currently undergoing treatment for alcohol and/or drug abuse.
  • Has received drugs that may interfere with bone metabolism within two weeks prior to the planned surgery date (e.g., steroids or methotrexate) excluding routine perioperative, non-steroidal anti-inflammatory drugs.
  • Has a history of autoimmune disease.
  • Has a history of exposure to injectable collagen implants.
  • Has a history of hypersensitivity to protein pharmaceuticals (monoclonal antibodies or gamma globulins) or collagen.
  • Has received treatment with an investigational therapy (device and/or pharmaceutical) within 30 days prior to surgery or such treatment is planned during the 24 months following surgery.
  • Has received any previous exposure to any/all BMPs of either human or animal extraction.
  • Has a history of allergy to bovine products or a history of general anaphylaxis.
  • Has a history of any endocrine or metabolic disorder known to affect osteogenesis (e.g., Paget's disease, renal oseodystrophy, Ehlos-Danlos syndrome or osteogenesis imperfecta).
  • Has any disease that would preclude accurate clinical evaluation (e.g., neuromuscular disease, etc.).
  • Has a primary diagnosis of a spinal disorder other than degenerative disc disease or other conditions as set out in "inclusions" above at the involved level(s).
  • Has a condition that requires postoperative medications that interfere with fusion, such as steroids or prolonged use of non-steroidal anti-inflammatory drugs, excluding routine perioperative non-steroidal anti-inflammatory drugs. This does not include low dose aspirin for prophylactic anticoagulation.
  • Has overt or active bacterial infection, local or systemic, and/or a potential for bacteremia.
  • Has presence of active malignancy or prior history of malignancy (except for basal cell carcinoma of the skin).
  • Has a documented metal allergy or intolerance to titanium alloy or cobalt-chrome-molybdenum alloy.
  • Is, in the opinion of the Principal Investigator or Co-Investigators, intellectually unable to co-operate with the study.
  • Has chronic or acute renal and/or hepatic failure or prior history of renal or hepatic disease.
Sexes Eligible for Study: All
18 Years to 75 Years   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
Australia,   Netherlands
EudraCT Number: 2009-012672-27
Not Provided
Not Provided
Baxter Healthcare Corporation
Baxter Healthcare Corporation
Apatech, Inc.
Study Director: Huub Kreuwel, Ph.D Director, Medical Affairs
Baxter Healthcare Corporation
April 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP