Non Fusion Surgery in Adolescent Idiopathic Scoliosis Patients (NEMOST-AIS)
Primary Purpose
Adolescent Idiopathic Scoliosis
Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
NEMOST system
Sponsored by
About this trial
This is an interventional treatment trial for Adolescent Idiopathic Scoliosis focused on measuring scoliosis, nonfusion, surgery, fusionless, idiopathic, adolescent
Eligibility Criteria
Inclusion Criteria:
- Adolescent idiopathic scoliosis ;
- Primary Cobb angle greater than 30°;
- Failed non-operative treatment defined as progression of the curve greater than 5° per year at any time;
- Skeletally immature (Risser grade* ≤1 and Skeletal age of hand and wrist X-rays ≤14y);
- In girl, either pre-menarchal or post-menarchal by no more than 1 year;
- Age over 10 years;
- Non rigid curve;
- All Lenke type;
- No previous spine surgery.
Exclusion Criteria:
- Non-idiopathic scoliosis: musculoskeletal or neurologic conditions responsible for cause of the spine curvature (i.e. neuromuscular, congenital or syndromic scoliosis);
- History of previous spine surgery;
- Risser sign >1;
- Disease or deformity likely to affect the stability of the device (i.e. inadequate anatomy of pedicles, trauma or tumor in fixation region, severe osteoporosis, bone destruction or poor bone quality);
- Non-reductible scoliosis;
- Known allergy or intolerance to one of the device material;
- Acute or chronic infections, local or systemic;
- Absence or insufficience of covering tissues;
- Pathological obesity.
Sites / Locations
- AmsterdamUMC, location AMCRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
NEMOST-AIS
Arm Description
This study is designed as a cohort study.
Outcomes
Primary Outcome Measures
Coronal balance (Correction of the primary curvature on radiograph
Cobb angle (degrees)
T1-S1 length on radiograph
length (cm)
instrument segment length on radiograph
length (cm)
(Serious) Adverse Event
complications
Sagittal balance (thoracic kyphosis, lumbar lordosis, proximal and distal junctional angle)
Cobb angle (degrees)
Pelvic parameters (pelvic obliquity, sacral slope, pelvic incidence, pelvic tilt)
degrees
Secondary Outcome Measures
Vertebral rotation
scoliometer assesment
Patient Reported Outcome (PRO
Scoliosis Research Society's-22 questionnaire
Full Information
NCT ID
NCT04441411
First Posted
June 11, 2020
Last Updated
June 18, 2020
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
1. Study Identification
Unique Protocol Identification Number
NCT04441411
Brief Title
Non Fusion Surgery in Adolescent Idiopathic Scoliosis Patients
Acronym
NEMOST-AIS
Official Title
Non Fusion Surgery in Adolescent Idiopathic Scoliosis Patients Using the Nemost-AIS System
Study Type
Interventional
2. Study Status
Record Verification Date
June 2020
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
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
The primary objective of the study is to monitor the effectiveness of a minimal invasive non-fusion double rod bipolar posterior spinal implant (Nemost growing domino) to correct the scoliotic curve in growing patients suffering from progressive adolescent idiopathic scoliosis (AIS) who have failed conservative treatment.
Detailed Description
Scoliosis is a complex three-dimensional deformity of the spine, which occurs primarily in growing children and adolescents. In adolescent idiopathic scoliosis (AIS), the cause is unknown. Children with severe and progressive scoliosis, if left untreated, are at risk of rapid and severe spinal deformity progression, which can result in a decrease of pulmonary function, poor cosmetic result and poor quality of life.
Treatment options in AIS depend on curve severity and remaining growth potential, and include intensive brace treatment for smaller curvatures whereas surgical correction and spinal fusion is advocated for more severe curves. Growing rods are used for severe early infantile deformities or early onset scoliosis (EOS).
Bracing, by using a rigid plastic orthosis, is currently the primary therapy to prevent curve progression in mild curves up to 45 degrees and skeletal immature patients. Most braces are recommended to be worn for 18-23 hours per day during several years (until skeletal maturity has been reached). This may cause a high level of physical discomfort and emotional and psychological stress in these patients, and failure of brace treatment therefore is common.
Surgical therapy for AIS is recommended in severe progressive curvatures. Surgical treatment includes correction of the spinal curvature by using multisegmental screw fixation and posterior spinal fusion of the thoracolumbar spine. Complete posterior spinal fusion, however, lacks the possibilities for future adaptation of natural changes in spinal balance and posture.
Currently, growing rods systems are used as a posterior spinal implant to allow growth of the spine and thorax and limit progression of the scoliosis in young patients with early onset scoliosis. Growing rods systems are distractible spinal implants, with bipolar anchorage fixations to the upper and lower part of the spine, using posterior spinal instrumentation such as hooks and pedicle screws.
The Nemost growing system, developed by the EUROS Compagny, is a CE-marked commercial available medical device for the treatment of early onset neuromuscular or early onset idiopathic scoliosis. It is a non-fusion, growth enabling system with bipolar fixation intended to be used with a posterior spinal instrumentation.
It is hypothesized that the use of a minimal invasive non-fusion bipolar posterior spinal implant (Nemost growing domino) can both correct and brace the spine internally and adapt balans and or distraction as the idiopathic scoliosis patient grows.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescent Idiopathic Scoliosis
Keywords
scoliosis, nonfusion, surgery, fusionless, idiopathic, adolescent
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Cohort study
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
NEMOST-AIS
Arm Type
Other
Arm Description
This study is designed as a cohort study.
Intervention Type
Device
Intervention Name(s)
NEMOST system
Intervention Description
Minimal invasive double rod posterior Non-Fusion Scoliosis Surgery
Primary Outcome Measure Information:
Title
Coronal balance (Correction of the primary curvature on radiograph
Description
Cobb angle (degrees)
Time Frame
2 years
Title
T1-S1 length on radiograph
Description
length (cm)
Time Frame
2 years
Title
instrument segment length on radiograph
Description
length (cm)
Time Frame
2 years
Title
(Serious) Adverse Event
Description
complications
Time Frame
2 years
Title
Sagittal balance (thoracic kyphosis, lumbar lordosis, proximal and distal junctional angle)
Description
Cobb angle (degrees)
Time Frame
2 years
Title
Pelvic parameters (pelvic obliquity, sacral slope, pelvic incidence, pelvic tilt)
Description
degrees
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Vertebral rotation
Description
scoliometer assesment
Time Frame
2 years
Title
Patient Reported Outcome (PRO
Description
Scoliosis Research Society's-22 questionnaire
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adolescent idiopathic scoliosis ;
Primary Cobb angle greater than 30°;
Failed non-operative treatment defined as progression of the curve greater than 5° per year at any time;
Skeletally immature (Risser grade* ≤1 and Skeletal age of hand and wrist X-rays ≤14y);
In girl, either pre-menarchal or post-menarchal by no more than 1 year;
Age over 10 years;
Non rigid curve;
All Lenke type;
No previous spine surgery.
Exclusion Criteria:
Non-idiopathic scoliosis: musculoskeletal or neurologic conditions responsible for cause of the spine curvature (i.e. neuromuscular, congenital or syndromic scoliosis);
History of previous spine surgery;
Risser sign >1;
Disease or deformity likely to affect the stability of the device (i.e. inadequate anatomy of pedicles, trauma or tumor in fixation region, severe osteoporosis, bone destruction or poor bone quality);
Non-reductible scoliosis;
Known allergy or intolerance to one of the device material;
Acute or chronic infections, local or systemic;
Absence or insufficience of covering tissues;
Pathological obesity.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
BJ Van Royen, MD, PhD
Phone
+31(0)5662672
Email
bj.vanroyen@amsterdamumc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
AMC AmsterdamUMC
Phone
+31(0)205669111
Email
amcfoundation@amc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
BJ Van Royen, MD, PhD
Organizational Affiliation
AmsterdamUMC
Official's Role
Principal Investigator
Facility Information:
Facility Name
AmsterdamUMC, location AMC
City
Amsterdam
State/Province
NH
ZIP/Postal Code
1105AZ
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dept of Orthopedics
Phone
+31(20)5662672
First Name & Middle Initial & Last Name & Degree
Dept of orthopaedics
Phone
+31(20)5662672
12. IPD Sharing Statement
Plan to Share IPD
No
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Non Fusion Surgery in Adolescent Idiopathic Scoliosis Patients
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