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Safety Outcomes of Vertebral Body Tethering Technique

Primary Purpose

Idiopathic Adolescent Scoliosis

Status
Suspended
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Anterior body tether (ABT)
Sponsored by
Nemours Children's Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Adolescent Scoliosis focused on measuring scoliosis, Vertebral Body Tethering, curve, Shah

Eligibility Criteria

8 Years - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Males or females age 8 to 16 years old at time of enrollment (inclusive)
  2. Diagnosis of idiopathic scoliosis
  3. Sanders bone age of less than or equal to 4
  4. Thoracic curve of greater than or equal to 35 degrees and less than or equal to 60 degrees
  5. Lumbar curve less than 35 degrees
  6. Patient has already been identified for and recommended to have surgical intervention
  7. Spina bifida occulta is permitted
  8. 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:

  1. Pregnancy (current)
  2. Prior spinal or chest surgery
  3. MRI abnormalities (including syrinx greater than 4mm, Chiari malformation, or tethered cord)
  4. Neuromuscular, thoracogenic, cardiogenic scoliosis, or any other non-idiopathic scoliosis
  5. Associated syndrome, including Marfan syndrome or neurofibromatosis
  6. Sanders bone age greater than 4
  7. Thoracic curve less than 35 degrees or greater than 60 degrees
  8. Lumbar curve greater than or equal to 35 degrees
  9. Unable or unwilling to firmly commit to returning for required follow-up visits
  10. Investigator judgement that the subject/family may not be a candidate for the intervention

Sites / Locations

  • Nemours Hospital for Children

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Anterior Vertebral Tethering

Arm Description

Anterior Vertebral Tether Vertebral body tethering done through anterior spine surgery under anesthesia.

Outcomes

Primary Outcome Measures

Number of adverse events after the procedure
We will look for any changes in neurological status, tether failure, implant reoperation, overcorrection and wound infections. Adverse events will be summarized by their severity and frequency and reported to IRB and Data Safety board on timely bases. The PI will determine if these events are related to the device.

Secondary Outcome Measures

Cobb angle in degrees
The difference be between pre and post-operative Cobb angle measurements.

Full Information

First Posted
September 27, 2019
Last Updated
May 8, 2023
Sponsor
Nemours Children's Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT04119284
Brief Title
Safety Outcomes of Vertebral Body Tethering Technique
Official Title
Safety and Efficacy of a Vertebral Body Tethering Technique for Pediatric Idiopathic Scoliosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Suspended
Why Stopped
IRB suspended the study.
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
September 1, 2025 (Anticipated)
Study Completion Date
September 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nemours Children's Clinic

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
The objectives of this study is to assess whether the intervention (Anterior Vertebral Tethering) is a safe and efficacious method of anterior approach surgery for spinal deformity in pediatric scoliosis.
Detailed Description
Scoliosis is a condition where the spine is deformed by a curvature in the coronal plane. It is generally associated with a twisting (axial plane) deformity as well. 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 Adolescent Idiopathic Scoliosis(AIS) 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 efficacy of Anterior Vertebral Body Tethering to avoid curve progression to more than 50 degrees.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Adolescent Scoliosis
Keywords
scoliosis, Vertebral Body Tethering, curve, Shah

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Anterior Vertebral Tethering
Arm Type
Experimental
Arm Description
Anterior Vertebral Tether Vertebral body tethering done through anterior spine surgery under anesthesia.
Intervention Type
Device
Intervention Name(s)
Anterior body tether (ABT)
Other Intervention Name(s)
Reflect/Transition™ Stabilization System Polyethylene terephthalate (PET) cord
Intervention Description
To insert the ABT in patients to correct AIS.
Primary Outcome Measure Information:
Title
Number of adverse events after the procedure
Description
We will look for any changes in neurological status, tether failure, implant reoperation, overcorrection and wound infections. Adverse events will be summarized by their severity and frequency and reported to IRB and Data Safety board on timely bases. The PI will determine if these events are related to the device.
Time Frame
2 years after the surgery
Secondary Outcome Measure Information:
Title
Cobb angle in degrees
Description
The difference be between pre and post-operative Cobb angle measurements.
Time Frame
Cobb angle will be measured prior to surgery, at 6 moths, 1 year and 2 years past surgery.

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
Suken Shah, MD
Organizational Affiliation
Nemours-AIDHC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nemours Hospital for Children
City
Wilmington
State/Province
Delaware
ZIP/Postal Code
19803
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Available IPD and Supporting Information:
Available IPD/Information Type
Informed Consent Form
Available IPD/Information URL
http://irbnet.org
Available IPD/Information Comments
The Informed consent form can be obtained while the patient is seen for scoliosis at Nemours-AIDHC.

Learn more about this trial

Safety Outcomes of Vertebral Body Tethering Technique

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