Vertebral Body Tethering Outcomes for Pediatric Idiopathic Scoliosis
Primary Purpose
Idiopathic Scoliosis
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Anterior Vertebral Tether
Sponsored by
About this trial
This is an interventional device feasibility trial for Idiopathic Scoliosis focused on measuring Scoliosis, Idiopathic Scoliosis, Adolescent Idiopathic Scoliosis
Eligibility Criteria
Inclusion Criteria:
- Males or females age 8 to 16 years old at time of enrollment (inclusive)
- Diagnosis of idiopathic scoliosis
- Sanders bone age of less than or equal to 4
- Thoracic curve of greater than or equal to 35 degrees and less than or equal to 60 degrees
- Lumbar curve less than 35 degrees
- Patient has already been identified for and recommended to have surgical intervention
- Spina bifida occulta is permitted
- Spondylolysis or Spondylolisthesis is permitted, as long as it is non-operative, the subject has not had any previous surgery for this, and no surgery is planned in the future
Exclusion Criteria:
- Pregnancy (current)
- Prior spinal or chest surgery
- MRI abnormalities (including syrinx greater than 4mm, Chiari malformation, or tethered cord)
- Neuromuscular, thoracogenic, cardiogenic scoliosis, or any other non-idiopathic scoliosis
- Associated syndrome, including Marfan syndrome or neurofibromatosis
- Sanders bone age greater than 4
- Thoracic curve less than 35 degrees or greater than 60 degrees
- Lumbar curve greater than or equal to 35 degrees
- Unable or unwilling to firmly commit to returning for required follow-up visits
- Investigator judgement that the subject/family may not be a candidate for the intervention
Sites / Locations
- The Children's Hospital of Philadelphia
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Anterior Vertebral Tethering
Arm Description
Subjects receiving Anterior Vertebral Tethering intervention.
Outcomes
Primary Outcome Measures
Incidence of Treatment-Emergent Adverse Events
Intra-operative and post-intervention medical events or signs and symptoms of complications arising after the start of study intervention will be captured. The event description, date of onset, end date, severity, and outcome will be documented. The frequencies, type, body system, severity, and relationship to the study intervention will also be summarized. A distinction will be made between those events which are "device-related" and "non device-related".
Secondary Outcome Measures
Comparison of Pre-Operative and Post-Operative Cobb Angle
The exploratory therapeutic endpoint used for feasibility will be change in post-operative Cobb angle compared to pre-operative Cobb angle, measured on coronal radiograph of the spine.
Comparison of Pre-Operative and Post-Operative SRS 30 Scores
The SRS 30 questionnaire will be administered at pre-operative and post-operative time points. The results of the questionnaire will be used for pre-operative and post-operative comparative analysis of device related outcomes.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03194568
Brief Title
Vertebral Body Tethering Outcomes for Pediatric Idiopathic Scoliosis
Official Title
Safety and Feasibility of a Vertebral Body Tethering Technique for Pediatric Idiopathic Scoliosis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 12, 2017 (Actual)
Primary Completion Date
January 26, 2022 (Actual)
Study Completion Date
May 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Patrick Cahill, MD
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will assess whether Anterior Vertebral Tethering is a safe and feasible method of anterior approach surgery for spinal deformity in pediatric idiopathic scoliosis.
Detailed Description
Scoliosis is a condition in which the spine is deformed by a curvature in the coronal plane. It is generally associated with a twisting (axial plane) deformity as well. It can have a variety of underlying etiologies and the etiology is used to classify the types of scoliosis. Idiopathic scoliosis is sub-classified in two ways: by age of onset and by magnitude of deformity. Curves between 10 and 25 degrees are considered mild. Curves between 25 and 50 degrees are classified as moderate. Curves greater than 50 degrees are termed severe. The current standard of care for moderate scoliosis in patients with remaining growth is to utilize a thoracolumbosacral orthosis (TLSO brace) to prevent progression of deformity. The scientific evidence has supported the efficacy of this intervention in avoiding progression of the Cobb angle to 50 degrees or more.
If treated with a TLSO brace, many idiopathic scoliosis patients would conceivably be subjected to years of brace wear and the cost and psychological factors inherent therein. Additional downsides of brace treatment include the potentially negative psychosocial impact of wearing an external sign of deformity during adolescence, a key period of emotional development. Prior research has identified negative psychosocial effects related to wearing a brace in children.
Recent evidence has suggested that certain curve patterns will likely progress to 50 degrees or more, despite treatment with a TLSO brace. Sanders, et al. demonstrated a correlation of Cobb angle (greater than 35 degrees) and skeletal maturity (bone age 4 or less) to the risk of progression to 50 degrees or more, despite TLSO bracing. The evidence supports that the current practice of TLSO bracing is not an effective treatment to avoid progression to 50 degrees in these patients. It is on this population (thoracic Cobb angle greater than 35 degrees, bone age of 4 or less) that we intend to test the safety and feasibility of Anterior Vertebral Body Tethering to avoid curve progression to 50 degrees.
The study intervention is surgical orthopedic implantation of the Anterior Vertebral Tether Device, by way of thoracoscopic surgery under general anesthesia. The primary outcome measures include assessments of safety of the insertion procedure and of the device, as well as the secondary measure of feasibility by determining the ability to successfully implant the investigational device.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Scoliosis
Keywords
Scoliosis, Idiopathic Scoliosis, Adolescent Idiopathic Scoliosis
7. Study Design
Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Anterior Vertebral Tethering
Arm Type
Experimental
Arm Description
Subjects receiving Anterior Vertebral Tethering intervention.
Intervention Type
Device
Intervention Name(s)
Anterior Vertebral Tether
Intervention Description
Vertebral body tethering through anterior thoracoscopic approach under general anesthesia and fluoroscopic guidance.
Primary Outcome Measure Information:
Title
Incidence of Treatment-Emergent Adverse Events
Description
Intra-operative and post-intervention medical events or signs and symptoms of complications arising after the start of study intervention will be captured. The event description, date of onset, end date, severity, and outcome will be documented. The frequencies, type, body system, severity, and relationship to the study intervention will also be summarized. A distinction will be made between those events which are "device-related" and "non device-related".
Time Frame
2 years after last subject's device implantation
Secondary Outcome Measure Information:
Title
Comparison of Pre-Operative and Post-Operative Cobb Angle
Description
The exploratory therapeutic endpoint used for feasibility will be change in post-operative Cobb angle compared to pre-operative Cobb angle, measured on coronal radiograph of the spine.
Time Frame
2 years after last subject's device implantation
Title
Comparison of Pre-Operative and Post-Operative SRS 30 Scores
Description
The SRS 30 questionnaire will be administered at pre-operative and post-operative time points. The results of the questionnaire will be used for pre-operative and post-operative comparative analysis of device related outcomes.
Time Frame
2 years after last subject's device implantation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males or females age 8 to 16 years old at time of enrollment (inclusive)
Diagnosis of idiopathic scoliosis
Sanders bone age of less than or equal to 4
Thoracic curve of greater than or equal to 35 degrees and less than or equal to 60 degrees
Lumbar curve less than 35 degrees
Patient has already been identified for and recommended to have surgical intervention
Spina bifida occulta is permitted
Spondylolysis or Spondylolisthesis is permitted, as long as it is non-operative, the subject has not had any previous surgery for this, and no surgery is planned in the future
Exclusion Criteria:
Pregnancy (current)
Prior spinal or chest surgery
MRI abnormalities (including syrinx greater than 4mm, Chiari malformation, or tethered cord)
Neuromuscular, thoracogenic, cardiogenic scoliosis, or any other non-idiopathic scoliosis
Associated syndrome, including Marfan syndrome or neurofibromatosis
Sanders bone age greater than 4
Thoracic curve less than 35 degrees or greater than 60 degrees
Lumbar curve greater than or equal to 35 degrees
Unable or unwilling to firmly commit to returning for required follow-up visits
Investigator judgement that the subject/family may not be a candidate for the intervention
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick Cahill, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Vertebral Body Tethering Outcomes for Pediatric Idiopathic Scoliosis
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