Clinical Outcome and Fusion Results Using the VerteLoc® Facet Fixation Device

NCT ID: NCT01892878

Last Updated: 2018-03-16

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-07-31
• Study Completion Date: 2016-01-01

Brief Summary

The purpose of this clinical study is to evaluate fusion of the facet joints in a prospective cohort of patients utilizing the VerteLoc facet fixation device in patients receiving lumbar laminectomy (L1-S1), without ancillary stabilization devices such as pedicle and transfacet screws.

Detailed Description

Study Design: Non-randomized, prospective, single arm clinical trial

Patient Population and Sample Size: Patients (n=25) from up to 2 clinical site, who have been medically evaluated, found appropriate for, and have agreed to treatment by lumbar decompressive laminectomy and facet fixation, including unilateral and/or bilateral posterolateral fusion according to accepted medical standards.

Objectives:

The primary objective of this study is to:

1. Evaluate the fusion status of facet joints following laminectomy and facet fixation using the VerteLoc system in combination with unilateral and/or bilateral posterolateral fusion.

2. Subject success / Clinical outcome: Evaluate the reduction in baseline VAS back pain score at 2-3 weeks, 3 months, and 12 months.

The secondary objectives of this study are to:

1. Explore the effect of preoperative bone density on facet fusion status;

2. Assess the ease of use of the VerteLoc system;

3. Record operative time using the VerteLoc system;

4. Monitor the occurrence of adverse events related or possibly related to the use of the VerteLoc system;

5. Monitor the occurrence of subsequent surgical intervention at the target level(s).

6. Subject success/Clinical outcome (Assess additional improvement criteria)

7. Evaluate Fusion rate in relations to DEXA value

Inclusion Criteria: Candidates must meet ALL of the following:

1. Have provided consent for research by signing the Institutional Review Board approved Informed Consent;

2. Have given appropriate operative consent for a decompressive lumbar (L1-S1) laminectomy procedure as standard of care;

3. Are skeletally mature, and are at least 18 years of age;

4. If female, are not pregnant;

5. Agree to adhere to post-surgical medically prescribed activity limitations and/or physical rehabilitation.

Exclusion Criteria:

1. Previous surgery at the target or adjacent vertebral levels;

2. More than two intervertebral levels to be treated by the laminectomy procedure;

3. Found to be inappropriate candidates for facet fixation using the VerteLoc system;

4. Require additional and/or other surgical technique and/or approach to the laminectomy at the index level(s), which may in the opinion of the Primary Investigator confound measurement of outcome variables;

5. Has a medical disorder or is receiving medications that would be expected to interfere with osteogeneses,

6. Active malignancy or patient with a history of any malignancy (except non-melanoma skin cancer) with recurrence within 5 years of surgery;

7. Active local or systemic infection or history of local or systemic infection, immune-deficiency, uncontrolled medical conditions, which in the opinion of the Investigator may increase patient risk or confound fusion results;

8. BMI >40% ;

9. History of tobacco smoking within the past 6 months;

10. Has a history of alcoholism, medication or drug abuse, psychosis, is a prisoner, and/or has a personality disorder, poor motivation, emotional or intellectual issues that would likely make the patient unreliable for participation in the study;

11. Are participating in any other clinical trial. Study Duration : 12 months

Study Outcomes:

The primary study outcomes of this study are:

1. Fusion grade at 12 month follow-up using CT scans with a grading system based on:

1. Complete fusion;

2. Partial fusion;

3. No fusion;

2. Subject success / Clinical outcome:

Evaluate the reduction in baseline VAS back pain score at:

1. 2-3 weeks

2. 3 months

3. 12 months.

The secondary outcomes of this study are:

1. Statistical correlation of DEXA scan bone mass density score to CT and radiographic fusion status;

2. Surgeon opinion of "ease of use" utilizing the VerteLoc system (0-10);

3. Operative time (minutes) from surgical access to completion of device placement

4. Occurrence and prevalence of adverse events related or possibly related to the use of the VerteLoc System;

5. Occurrence of subsequent surgical intervention at the target level(s).

Study Assessments

• Intraoperative: Post-placement radiograph;
• 12 months: A/P and lateral flexion and extension lumbar radiograph and lumbar CT scan.

Statistical Analysis

• Student t-tests

Conditions

Spinal Stenosis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Single Arm Study

All patients will receive treatment

Group Type: OTHER

VerteLoc

Intervention Type: PROCEDURE

Single Arm

Interventions

VerteLoc

Single Arm

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Have provided consent for research by signing the Institutional Review Board approved Informed Consent;

2. Have given appropriate operative consent for a decompressive lumbar (L1-S1) laminectomy procedure as standard of care;

3. Are skeletally mature, and are at least 18 years of age;

4. If female, are not pregnant;

5. Agree to adhere to post-surgical medically prescribed activity limitations and/or physical rehabilitation.

Exclusion Criteria

1. Previous surgery at the target or adjacent vertebral levels;

2. More than two intervertebral levels to be treated by the laminectomy procedure;

3. Found to be inappropriate candidates for facet fixation using the VerteLoc system;

4. Require additional and/or other surgical technique and/or approach to the laminectomy at the index level(s), which may in the opinion of the Primary Investigator confound measurement of outcome variables;

5. Has a medical disorder or is receiving medications that would be expected to interfere with osteogeneses,

6. Active malignancy or patient with a history of any malignancy (except non-melanoma skin cancer) with recurrence within 5 years of surgery;

7. Active local or systemic infection or history of local or systemic infection, immune-deficiency, uncontrolled medical conditions, which in the opinion of the Investigator may increase patient risk or confound fusion results;

8. BMI >40% ;

9. History of tobacco smoking within the past 6 months;

10. Has a history of alcoholism, medication or drug abuse, psychosis, is a prisoner, and/or has a personality disorder, poor motivation, emotional or intellectual issues that would likely make the patient unreliable for participation in the study;

11. Are participating in any other clinical trial.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

VG Innovations, LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Lisa Guyot, MD

Role: PRINCIPAL_INVESTIGATOR

Ascension Health

Locations

Genesys Regional Medical Center

Grand Blanc, Michigan, United States

Countries

United States

Other Identifiers

VGI-002

Identifier Type: -

Identifier Source: org_study_id