CopiOs Posterolateral Fusion Procedure

Phase 2

Terminated

• Conditions: Spondylolisthesis; Stenosis
• Interventions: Device: Copios

• Registration Number: NCT01123850
• Lead Sponsor: Zimmer Biomet

Brief Summary

To compare radiographic data collection from patients undergoing instrumented PLF with CopiOs(R) BVF or instrumented PLF with autologous bone and to assess overall clinical outcomes. Patients will serve as self controls.

Detailed Description

This is a prospective, counter-balanced study involving 85 subjects at up to 8 investigative centers. Each subject will be an appropriate candidate for an instrumented PLF and will meet the inclusion and exclusion criteria. All subjects will undergo an instrumented, pedicle screw PLF procedure. Autograft or other interbody devices identified by the surgeon to be in the best interest of the patient may be used. Enrolled patients will receive CopiOs BVF sponge soaked with bone marrow aspirate on one side and autologous bone on the other side. All patients will receive both CopiOs BVF and autologous bone. Patients will serve as self-controls in this counter-balanced study. Data will be collected pre-operatively, operatively and post-operatively at six and twelve months.

The study objectives include: Radiographic success of CopiOs is non-inferior to autograft with clear evidence of bridging bone. Radiographic analysis will be used to show that CopiOs works as well as autograft when comparing the rate of fusion at 6 and 12 months. The CT scan (12 month) will show that CopiOs works as well as autograft when comparing the fusion mass between the transverse processes. Additionally, clinical success will be determined by an improvement of 15 percentage points using the Oswestry Disability Index and maintenance or improvement in the motor and sensory components of the neurological assessment from preoperative to postoperative. Since patients serve as self-controls there will be no clinical success comparisons between the groups. Rather, clinical success will be measured on overall improvement based on patient outcomes.

Study Timeline

• Study First Submitted: 2010-05-12
• Study First Submitted QC: 2010-05-13
• Study First Posted: 2010-05-14
• Study Start: 2010-06
• Primary Completion: 2012-10
• Study Completion: 2012-10
• Results First Submitted: 2015-04-24
• Status Verified: 2015-05
• Results First Submitted QC: 2015-05-11
• Last Update Submitted: 2015-05-11
• Results First Posted: 2015-05-27
• Last Update Posted: 2015-05-27

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

• Patient must be skeletally mature; between the ages of 21 and 75
• Patients having degenerative spondylolisthesis, stenosis with instability, or degenerative disc disease as diagnosed by radicular signs and/or imaging studies
• Patients will be medically indicated for a single-level, instrumented PLF between L2 and S1 per their surgeon
• Patient must be willing and able to comply with study requirements, including all necessary study related paperwork and follow-up visits

Exclusion Criteria

• Use of iliac crest bone graft;
• Any previous lumbar spinal surgeries at indicated level;
• Any medical or physical condition that would preclude the potential benefit of spinal surgery;
• Use of a dynamic stabilization systems;
• Sites where stresses on void will exceed the load strength of fixation of hardware;
• Segmental defects;
• Significantly impaired vascularity proximal to the surgical site;
• Sites in direct contact with articular space;
• Soft tissue deficit not allowing closure;
• Active systemic or local infection;
• Severe degenerative bone disease;
• Patients with osteoporosis who are actively under treatment;
• Extreme obesity, as defined by NIH Clinical Guidelines Body Mass Index (BMI>40 kg/m2);
• Active malignancy;
• Patients with a history of multiple allergies;
• Patients with known allergies to bovine collagen;
• Hypercalcemia;
• Pregnancy;
• Mental illness;
• Alcohol or drug abuse;
• Incarceration.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Single ARM - Copios Bone Filler	Copios	All subjects will undergo an instrumented, pedicle screw PLF procedure. Autograft or other interbody devices identified by the surgeon to be in the best interest of the patient may be used. Enrolled patients will receive CopiOs BVF sponge soaked with bone marrow aspirate on one side and autologous bone on the other side. All patients will receive both CopiOs BVF and autologous bone. Patients will serve as self-controls in this counter-balanced study.

Primary Outcome Measures

Name	Time	Method
Fusion Assessment	6 M, 12 M	Fusion at 12M using radiograph Fusion Mass at 12M using CT

Secondary Outcome Measures

Name	Time	Method
Outcome Measure - Pain, Life Quality, Satisfaction	PreOp, Surgery, 6M, 12M

Trial Locations

Locations (6)

Las Cruces Orthopaedic Associates; 🇺🇸 Las Cruces, New Mexico, United States

Neurological Surgery of Southern Illinois; 🇺🇸 Belleville, Illinois, United States

Florida Hospital; 🇺🇸 Orlando, Florida, United States

Indiana Orthopedic Center; 🇺🇸 Indianapolis, Indiana, United States

Upstate Bone and Joint Center; 🇺🇸 East Syracuse, New York, United States

Scott and White Healthcare; 🇺🇸 Temple, Texas, United States