Carbon PEEK Versus Titanium Pedicle Screws in the Treatment of Spinal Tumors
Primary Purpose
Spinal Tumor
Status
Withdrawn
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
surgical stabilization of the spine due to primary and secondary spinal tumors
Sponsored by
About this trial
This is an interventional treatment trial for Spinal Tumor
Eligibility Criteria
Inclusion Criteria:
- Patients 18 to 99 years of Age
- Primary and secondary spinal tumors of the thoracolumbar spine requiring posterior instrumentation and radiation therapy
Exclusion Criteria:
- Need of cement augmentation or anterior cage support (corpectomy)
- Patients with contraindication against surgical resection
- Patients with incomplete medical records or insufficient imaging
Sites / Locations
- University Hospital Balgrist
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Instrumentation with Carbon/PEEK pedicle screw system
Instrumentation with titanium pedicle screw system
Arm Description
Posterior instrumentation using a Carbon/PEEK pedicle screw system two levels above and below the affected segment(s). The medical device is a commercial product, bears a conformity marking and is used in accordance with the instructions.
Posterior instrumentation using a titanium pedicle screw system two levels above and below the affected segment(s). The medical device is a commercial product, bears a conformity marking and is used in accordance with the instructions.
Outcomes
Primary Outcome Measures
radiation dose
The total radiation dose administered is measured in Gray
feasibility of planning the radiation therapy
evaluated by a subjective score (0-10) stated by an independent radiooncologist using a visual analogue scale from 0 to 10
Secondary Outcome Measures
radiological visualization of the area of interest
evaluated by a subjective score stated by an independent radiologist using a visual analogue scale from 0 to 10
time to recurrence
monitoring of recurrence using radiological imaging is performed routinely according to clinical standards
Full Information
NCT ID
NCT03893110
First Posted
February 4, 2019
Last Updated
April 28, 2020
Sponsor
Balgrist University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03893110
Brief Title
Carbon PEEK Versus Titanium Pedicle Screws in the Treatment of Spinal Tumors
Official Title
Carbon PEEK Versus Titanium Pedicle Screws in the Treatment of Spinal Tumors - A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Withdrawn
Why Stopped
Absence of Co-investigator
Study Start Date
June 27, 2018 (Actual)
Primary Completion Date
January 31, 2022 (Anticipated)
Study Completion Date
March 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Balgrist University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Radiation therapy is a cornerstone in the treatment of spinal neoplasms as radical resections are often limited anatomically. Frequently, a surgical stabilization with implants is required. However, metallic implants not only make the CT-based planning of a subsequent radiation therapy more difficult, but might also have an uncontrolled dose modulating effect in adjuvant radiotherapy. At the spine, radiation is limited by the effective dose posed to the relatively radiosensitive spinal cord. While metallic implants might result in an inhomogeneous and uncontrollable dose distribution due to the interface effect, the use of new radiolucent implants consisting of carbon/polyether ether ketone (PEEK) might allow a more homogeneous and predictable dose distribution. This study aims to evaluate the potential benefits of the use of carbon/PEEK pedicle screws during adjuvant radiation therapy and follow-up imaging of spinal tumors.
60 patients will randomized 1:1 into either treatment arm (Pedicle System Carbon/PEEK vs. Pedicle System Titanium). The feasibility of planning the radiation therapy will be evaluated. The postoperatively administered total radiation dose is documented. The radiological visualization of the area of interest will be evaluated The surgical outcome is evaluated by fusion rate, implant integrity and anchorage. Patients will be followed up for 12 months according to local standards.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Tumor
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Instrumentation with Carbon/PEEK pedicle screw system
Arm Type
Experimental
Arm Description
Posterior instrumentation using a Carbon/PEEK pedicle screw system two levels above and below the affected segment(s). The medical device is a commercial product, bears a conformity marking and is used in accordance with the instructions.
Arm Title
Instrumentation with titanium pedicle screw system
Arm Type
Active Comparator
Arm Description
Posterior instrumentation using a titanium pedicle screw system two levels above and below the affected segment(s). The medical device is a commercial product, bears a conformity marking and is used in accordance with the instructions.
Intervention Type
Procedure
Intervention Name(s)
surgical stabilization of the spine due to primary and secondary spinal tumors
Intervention Description
Posterior instrumentation with pedicle screw system
Primary Outcome Measure Information:
Title
radiation dose
Description
The total radiation dose administered is measured in Gray
Time Frame
within 6 weeks of radiation therapy
Title
feasibility of planning the radiation therapy
Description
evaluated by a subjective score (0-10) stated by an independent radiooncologist using a visual analogue scale from 0 to 10
Time Frame
before radiation therapy
Secondary Outcome Measure Information:
Title
radiological visualization of the area of interest
Description
evaluated by a subjective score stated by an independent radiologist using a visual analogue scale from 0 to 10
Time Frame
during radiation therapy
Title
time to recurrence
Description
monitoring of recurrence using radiological imaging is performed routinely according to clinical standards
Time Frame
up to 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients 18 to 99 years of Age
Primary and secondary spinal tumors of the thoracolumbar spine requiring posterior instrumentation and radiation therapy
Exclusion Criteria:
Need of cement augmentation or anterior cage support (corpectomy)
Patients with contraindication against surgical resection
Patients with incomplete medical records or insufficient imaging
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mazda Farshad, Prof.
Organizational Affiliation
Balgrist University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Balgrist
City
Zürich
State/Province
Zurich
ZIP/Postal Code
8008
Country
Switzerland
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
IPD only available to study personnel. statistical analysis will be done with encoded data only. study results will be published
Learn more about this trial
Carbon PEEK Versus Titanium Pedicle Screws in the Treatment of Spinal Tumors
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