Evaluation of DTRAX Graft in Patients With Cervical Degenerative Disc Disease

Not Applicable

Withdrawn

• Conditions: Cervical Radiculopathy; Cervical Spondylosis; Cervical Degenerative Disc Disease
• Interventions: Device: DTRAX Graft

• Registration Number: NCT01616719
• Lead Sponsor: Providence Medical Technology, Inc.

Brief Summary

DTRAX Graft is used to relieve nerve pressure in the neck in order to provide relief for Cervical Degenerative Disc Disease. This study is being conducted to determine the effectiveness of the graft, and to find out whether or not it provides better results or faster healing than traditional ways of performing surgery for Cervical Degenerative Disc Disease.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-05
• Study First Submitted: 2012-06-07
• Study First Submitted QC: 2012-06-08
• Study First Posted: 2012-06-12
• Primary Completion: 2014-02
• Study Completion: 2015-02
• Status Verified: 2020-03
• Last Update Submitted: 2020-03-02
• Last Update Posted: 2020-03-04

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

1. Subject diagnosed with DDD in C3-C7, defined as follows:

   • Radiographically (at least one):

     • degenerated disc on MRI;
     • decreased disc height on plain film, CT or MRI; and/or
     • disc herniation, as demonstrated by CT or MRI.

   • Clinically: radicular symptoms (at least one):

     • arm/shoulder pain;
     • decreased reflexes;
     • decreased strength; and/or
     • decreased sensation.

2. Subject has single-level disease, OR multi-level disease demonstrated radiographically, and confirmed to be symptomatic by one of the following methods:

   • Selective nerve root block, OR
   • EMG, OR
   • Distinctive clinical examination.

3. Subject has dynamic stenosis relieved by traction and made worse by a Spurlings maneuver.

4. Subject is 35-80 years of age, inclusive.

5. Subject is unresponsive to 6 weeks conservative, nonoperative treatment, or has the presence of progressive symptoms or signs of nerve root compression in face of combined nonoperative management.

6. Preoperative NDI score of ≥ 30.

7. Preoperative neck pain and arm pain score of ≥ 6 on Neck and Arm Pain Scales.

8. Patient is a male or non-pregnant, non-lactating female.

9. Female patients of child-bearing potential, including those who have had a tubal ligation, but excluding those who have not experienced a menstrual period for at least two years, must have a negative urine pregnancy test at Screening.

10. Patient must voluntarily provide written, informed consent.

11. Subject is able to meet the proposed follow-up schedule.

12. Subject is able to follow the postoperative management program.

Exclusion Criteria

1. Subject has severe osteopenia, osteoporosis, osteomalacia, spinal metastases, or metabolic bone disease OR the level of BMD is a T score of -2.5 or below OR patient has sustained a vertebral compression or nontraumatic hip or wrist fracture.
2. Subject has overt or active spinal and/or systemic infection.
3. Subject has spondylolisthesis ≥ 3.5mm or rotator subluxation.
4. Subject has cervical myelopathy.
5. Subject has a chronic pain syndrome.
6. Subject has radicular findings with major motor impairment.
7. Subject has a condition that requires postoperative medications that interfere with fusion or the stability of the implant, such as steroids.
8. Subject is mentally incompetent.
9. Subject is a prisoner.
10. Subject is pregnant.
11. Subject abuses alcohol or drugs.
12. Subject has a cervical spinal condition other than symptomatic cervical disc disease requiring surgical treatment at the involved level.
13. Subject has insulin dependent diabetes.
14. Subject has chronic or acute renal failure or prior history of renal disease.
15. Subject has fever at the time of surgery, defined as > 38.5 degrees C.
16. Subject has documented allergy or intolerance to stainless steel, titanium, or a titanium alloy.
17. Subject has received drugs which may interfere with bone metabolism within two weeks prior to the planned date of DTRAX surgery.
18. Subject has history of an endocrine or metabolic disorder known to affect osteogenesis .
19. Subject has had treatment with an investigational therapy within 28 days prior to DTRAX surgery or such treatment is planned during the 16 weeks following implantation of DTRAX Graft.
20. Subject is involved in spinal litigation or Workmen's Compensation claim.
21. Subject is obese, defined as body mass index (BMI) > 35.
22. Patient has psychiatric history, head injury or any other condition, which, in the Investigator's opinion, would prevent the patient from complying with postoperative follow-up visits.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
DTRAX graft	DTRAX Graft	-

Primary Outcome Measures

Name	Time	Method
Gather clinical outcome data on DTRAX Graft.	Baseline throughout 12 months post-operatively	Clinical outcome data will be collected using the Neck Disability Index (NDI), Visual Analogue Scale (VAS), and a quality of life questionnaire.

Secondary Outcome Measures

Name	Time	Method
Safety information will be evaluated by collecting the type, frequency, severity, device, and procedure-relatedness of adverse events.	Baseline throughout 12 months post-operatively

Trial Locations

Locations (2)

Office of Dr. Brian Andrews, Neurosurgery; 🇺🇸 San Francisco, California, United States

Neurospine Institute Medical Group; 🇺🇸 San Francisco, California, United States