INFUSE™ BONE GRAFT/CORNERSTONE-SR™ Allograft Ring/ATLANTIS™ Anterior Cervical Plate- Pilot Study

Not Applicable

Completed

• Conditions: Degenerative Cervical Disc Disease
• Interventions: Device: Autogenous bone/CORNERSTONE-SR™ /ATLANTIS™; Device: INFUSE™ Bone Graft/CORNERSTONE-SR™ /ATLANTIS™

• Registration Number: NCT01491399
• Lead Sponsor: Medtronic Spinal and Biologics

Brief Summary

The purpose of this clinical trial is to assess the safety and effectiveness of the Investigational implant as compared to the Control implant in the treatment of patients with one level or two adjacent levels of cervical symptomatic degenerative disc disease.

Detailed Description

Not available

Study Timeline

• Study Start: 1999-09
• Primary Completion: 2003-03
• Study Completion: 2003-03
• Study First Submitted: 2011-12-12
• Study First Submitted QC: 2011-12-13
• Study First Posted: 2011-12-14
• Status Verified: 2023-05
• Last Update Submitted: 2023-05-16
• Last Update Posted: 2023-05-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 33

Inclusion Criteria

1. Cervical disc disease defined as: intractable radiculopathy and/or myelopathy with at least one of the following items producing symptomatic nerve root and/or spinal cord compression which is documented by diagnostic imaging procedures:

   • herniated disc;
   • osteophyte formation;
   • decreased disc height;
   • thickening of ligamentous tissue;
   • disc degeneration; and/or
   • facet joint degeneration.

2. Has preoperative Neck Disability Index score >= 30;

3. C2-C3 disc to C7-Tl disc level(s) of involvement.

4. One or two adjacent levels requiring fusion;

5. No previous surgical intervention at the involved fusion level(s);

6. Unresponsive to nonoperative treatment for approximately six weeks or has the presence of progressive symptoms or signs of nerve root or spinal cord compression in face of continued nonoperative management;

7. Age > 18 years at time of surgery;

8. Is female of child-bearing potential, who is not pregnant or nursing, and who agrees to not get pregnant for 1 year following surgery;

9. Willingness to comply with study plan and sign the consent form.

Exclusion Criteria

1. Has cervical spinal condition requiring surgical treatment other than symptomatic cervical disc disease at the involved level(s).
2. Has been previously diagnosed with osteopenia, osteoporosis, or osteomalacia to a degree that anterior plating would be contraindicated.
3. Has presence of spinal metastases.
4. Has overt or active bacterial infection, either local or systemic.
5. Has fever (temperature > 101°F oral) at the time of surgery.
6. Has a documented titanium alloy allergy or intolerance.
7. Is mentally incompetent. If questionable, obtain psychiatric consult.
8. Is a prisoner.
9. Is an alcohol and/or drug abuser as defined by currently undergoing treatment for alcohol and/or drug usage.
10. Has received drugs which may interfere with bone metabolism within two weeks prior to the planned date of spinal fusion surgery (e.g., steroids or methotrexate), excluding routine perioperative anti-inflammatory drugs.
11. Has a history of autoimmune disease (Systemic Lupus Erythematosus or Dermatomyositis).
12. Has a history of exposure to injectable collagen implants.
13. Has a history of hypersensitivity to protein pharmaceuticals (monoclonal antibodies or gamma globulins) or collagen.
14. Has received treatment with an investigational therapy within 28 days prior to implantation surgery or such treatment is planned during the 16 weeks following rhBMP-2/ACS implantation.
15. Has received any previous exposure to any/all BMP's of either human or animal extraction.
16. Has a history of allergy to bovine products or a history of anaphylaxis.
17. Has history of endocrine or metabolic disorder known to affect osteogenesis (e.g., Paget's disease, renal osteodystrophy, Ehlers- Danlos syndrome, or osteogenesis imperfecta).
18. Has a condition which requires postoperative medications that interfere with fusion, such as steroids, excluding routine perioperative anti-inflammatory drugs.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Autogenous bone/CORNERSTONE-SR™	Autogenous bone/CORNERSTONE-SR™ /ATLANTIS™	-
INFUSE™ Bone Graft/CORNERSTONE-SR™	INFUSE™ Bone Graft/CORNERSTONE-SR™ /ATLANTIS™	-

Primary Outcome Measures

Name	Time	Method
Pain/Disability Status	24 month	The self-administered Neck Disability Index will be used. Success for each individual patient will be defined as pain/disability improvement postoperatively according to the following definition: Preoperative Score - Postoperative Score \>= 15
Fusion	24 month	Fusion is defined as: * No evidence of motion as defined by: less than 4° difference in angular motion between flexion and extension as seen on the lateral flexion/extension radiographs.; * No radiolucency greater than 2mm of thickness covering more than 50% of superior or inferior graft surface.; * Evidence of bridging trabecular bone.
Neurological Status	24 month	Neurological status will be assessed preoperatively and postoperatively using a comprehensive neurological status scale.

Secondary Outcome Measures

Name	Time	Method
Hip (Donor Site) Pain	24 month
Patient Global Perceived Effect	24 month
Time to fusion	24 month
General Health Status (SF-36)	24 month
Patient Satisfaction	24 month
Pain Status (neck pain, arm pain)	24 month