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Dysport ® as an Adjunctive Treatment to Bracing in the Management of Adolescent Idiopathic Scoliosis

Primary Purpose

Adolescent Idiopathic Scoliosis

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
AbobotulinumtoxinA
Placebos
Custom Thoracolumbosacral Orthosis
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adolescent Idiopathic Scoliosis focused on measuring AIS, adolescent idiopathic scoliosis

Eligibility Criteria

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

Inclusion criteria:

  • Clinically determined idiopathic nature of scoliosis
  • Age 10-16 years
  • Risser stage 0,1,or 2
  • major curve of 20°-40°
  • curve apex caudal to T7 vertebra
  • ability to adhere to bracing protocol
  • Botulinum toxin naïve or previously treated greater than 6 months prior to study entry

Exclusion criteria:

  • Diagnosis of congenital scoliosis, neuromuscular scoliosis, or other "reason" for scoliosis - Previous surgery at any segment of the spine
  • Current need for surgery at any level of the spine
  • Treatment with any drug known to interfere with neuromuscular function
  • Any other medical condition, laboratory or diagnostic procedure finding that might preclude administration of BTX
  • Ongoing infection at the injection sites
  • Diagnosis as either resistant or sensitive to botulinum toxin treatment of any type or to any components of the BTX formulation
  • Cow milk protein allergy

Sites / Locations

  • Johns Hopkins UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Botulinum Toxin

Placebo

Arm Description

The investigators plan to administer approximately 1000 U Dysport ® in the concave-sided paraspinal musculature of the major curve, based on an estimated total dose of 1000 U, the maximum allowable dose. The total dose per treatment session will not exceed 15 units/kilogram or 1000 units, whichever is lower. If two curves are equivalent within 3˚, both will be treated, however, the dosing (described above) will be divided equally across both curves. There will be two cycles of injections. Patients will be treated at time 0 (baseline) and 4 months.

Control patients will receive an injection of placebo specifically prepared as a control for this study. The same volumes as indicated in the "experimental" arm description will be injected. These will be administered during two cycles of injections. Patients will be treated at time 0 (baseline) and 4 months.

Outcomes

Primary Outcome Measures

Change in scoliotic curve as assessed by the Major Curve Cobb Angle
Change in scoliotic curve will be assessed using by the Major Curve Cobb Angle with measurement of standing scoliosis radiographs. Cobb angle refers to a radiographic measurement of side to side spinal curvature, measured in angle degrees.

Secondary Outcome Measures

Change in Patient Reported Outcomes
This will be assessed by Scoliosis Research Society (SRS) 22 Survey; The SRS-22 questionnaire is a validated measure used to assesses quality of life in patients with idiopathic scoliosis. It consists of five domains that assess: function, pain, mental health, self-image, and satisfaction with treatment. Higher scores indicate increased satisfaction. Each of the 22 questions are scored on a scale of 1 to 5.

Full Information

First Posted
April 30, 2019
Last Updated
April 13, 2023
Sponsor
Johns Hopkins University
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1. Study Identification

Unique Protocol Identification Number
NCT03935295
Brief Title
Dysport ® as an Adjunctive Treatment to Bracing in the Management of Adolescent Idiopathic Scoliosis
Official Title
Dysport ® (abobotulinumtoxinA) as an Adjunctive Treatment to Bracing in the Management of Adolescent Idiopathic Scoliosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 3, 2020 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
March 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
This study evaluates the combined effect of botulinum toxin A (administered as Dysport® (Ipsen Pharmaceuticals)) and bracing in children with adolescent idiopathic scoliosis. Two thirds of patients will be treated with Dysport® and bracing, while the remaining patients will be treated with placebo and bracing.
Detailed Description
Adolescent idiopathic scoliosis (AIS) is lateral curvature of the spine with an unknown cause in children 10-16 years old. Without treatment, skeletally immature children with idiopathic curves of 20°-40° risk curve progression. Treatment of these patients is focused on either observation or bracing. Although bracing has been shown to be more effective than observation, success is contingent on patient adherence and has the potential for further optimization with adjunct therapies. Little research is available concerning adjunct therapies that may be used during bracing of AIS patients. One therapy in particular, abobotulinumtoxinA (BTX) injection, has been poorly studied. Injection of BTX into the paraspinal musculature of the concave aspect of the major curve may result in a more malleable curve and thus optimize brace treatment. If BTX injections are found to improve outcomes in this way, a new standard of nonoperative care could be established for AIS patients, potentially reducing the number of patients who undergo surgery. The aim of this study is to assess whether BTX injections (administered as Dysport® (Ipsen Pharmaceuticals)) in the paraspinal musculature at the site of the major scoliotic curve decrease curve progression in skeletally immature AIS patients who are concurrently treated with bracing. Dysport® will be evaluated primarily as an adjunct treatment to bracing. Hypotheses Dysport® injections into the concave-side paraspinal muscles will decrease the rate of curve progression, with a lower rate of curve progression in patients treated with both Dysport® injections and bracing compared with those treated with only bracing. Quantitative physical and mental health scores will improve to a greater extent in patients treated with Dysport® and bracing compared with patients treated with only bracing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescent Idiopathic Scoliosis
Keywords
AIS, adolescent idiopathic scoliosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Botulinum Toxin
Arm Type
Experimental
Arm Description
The investigators plan to administer approximately 1000 U Dysport ® in the concave-sided paraspinal musculature of the major curve, based on an estimated total dose of 1000 U, the maximum allowable dose. The total dose per treatment session will not exceed 15 units/kilogram or 1000 units, whichever is lower. If two curves are equivalent within 3˚, both will be treated, however, the dosing (described above) will be divided equally across both curves. There will be two cycles of injections. Patients will be treated at time 0 (baseline) and 4 months.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Control patients will receive an injection of placebo specifically prepared as a control for this study. The same volumes as indicated in the "experimental" arm description will be injected. These will be administered during two cycles of injections. Patients will be treated at time 0 (baseline) and 4 months.
Intervention Type
Drug
Intervention Name(s)
AbobotulinumtoxinA
Other Intervention Name(s)
Dysport, Ipsen
Intervention Description
Paraspinal abobotulinumtoxinA injections (compared to placebo)
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
Placebo prepared by Ipsen for use as control
Intervention Type
Device
Intervention Name(s)
Custom Thoracolumbosacral Orthosis
Intervention Description
Non-operative external bracing for scoliosis curves
Primary Outcome Measure Information:
Title
Change in scoliotic curve as assessed by the Major Curve Cobb Angle
Description
Change in scoliotic curve will be assessed using by the Major Curve Cobb Angle with measurement of standing scoliosis radiographs. Cobb angle refers to a radiographic measurement of side to side spinal curvature, measured in angle degrees.
Time Frame
Assessed at baseline (time 0), 6 weeks, 4 months, 4 months + 6 weeks, 8 months
Secondary Outcome Measure Information:
Title
Change in Patient Reported Outcomes
Description
This will be assessed by Scoliosis Research Society (SRS) 22 Survey; The SRS-22 questionnaire is a validated measure used to assesses quality of life in patients with idiopathic scoliosis. It consists of five domains that assess: function, pain, mental health, self-image, and satisfaction with treatment. Higher scores indicate increased satisfaction. Each of the 22 questions are scored on a scale of 1 to 5.
Time Frame
Assessed at baseline (time 0), 6 weeks, 4 months, 4 months + 6 weeks, 8 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Clinically determined idiopathic nature of scoliosis Age 10-16 years Risser stage 0,1,or 2 major curve of 20°-40° curve apex caudal to T7 vertebra ability to adhere to bracing protocol Botulinum toxin naïve or previously treated greater than 6 months prior to study entry Exclusion criteria: Diagnosis of congenital scoliosis, neuromuscular scoliosis, or other "reason" for scoliosis - Previous surgery at any segment of the spine Current need for surgery at any level of the spine Treatment with any drug known to interfere with neuromuscular function Any other medical condition, laboratory or diagnostic procedure finding that might preclude administration of BTX Ongoing infection at the injection sites Diagnosis as either resistant or sensitive to botulinum toxin treatment of any type or to any components of the BTX formulation Cow milk protein allergy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gabrielle Reichard, MA
Phone
4105023626
Email
greicha1@jhmi.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Varun Puvanesarajah, MD
Phone
9193605646
Email
vpuvane1@jhmi.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Sponseller, MD, MBA
Organizational Affiliation
Johns Hopkins Hospital Department of Orthopaedic Surgery
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Varun Puvanesarajah, MD
Organizational Affiliation
Johns Hopkins Hospital Department of Orthopaedic Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Varun Puvanesarajah, MD
Phone
410-955-3136
Email
vpuvane1@jhmi.edu
First Name & Middle Initial & Last Name & Degree
Gabrielle Reichard, MA
Phone
4105023626
Email
greicha1@jh.edu
First Name & Middle Initial & Last Name & Degree
Paul D Sponseller, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23445094
Citation
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Results Reference
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16759428
Citation
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Results Reference
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PubMed Identifier
3810292
Citation
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Results Reference
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PubMed Identifier
26582623
Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
9240788
Citation
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Results Reference
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PubMed Identifier
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Citation
Wong C, Gosvig K, Sonne-Holm S. The role of the paravertebral muscles in adolescent idiopathic scoliosis evaluated by temporary paralysis. Scoliosis Spinal Disord. 2017 Oct 10;12:33. doi: 10.1186/s13013-017-0138-7. eCollection 2017.
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PubMed Identifier
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Citation
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Citation
Wong C. Mechanism of right thoracic adolescent idiopathic scoliosis at risk for progression; a unifying pathway of development by normal growth and imbalance. Scoliosis. 2015 Jan 27;10:2. doi: 10.1186/s13013-015-0030-2. eCollection 2015.
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PubMed Identifier
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Citation
RIDDLE HF, ROAF R. Muscle imbalance in the causation of scoliosis. Lancet. 1955 Jun 18;268(6877):1245-7. doi: 10.1016/s0140-6736(55)91020-5. No abstract available.
Results Reference
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PubMed Identifier
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Citation
Fidler MW, Jowett RL. Muscle imbalance in the aetiology of scoliosis. J Bone Joint Surg Br. 1976 May;58(2):200-1. doi: 10.1302/0301-620X.58B2.932082.
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PubMed Identifier
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Citation
Asher M, Min Lai S, Burton D, Manna B. The reliability and concurrent validity of the scoliosis research society-22 patient questionnaire for idiopathic scoliosis. Spine (Phila Pa 1976). 2003 Jan 1;28(1):63-9. doi: 10.1097/00007632-200301010-00015.
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Citation
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Citation
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Citation
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Results Reference
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Links:
URL
http://ipsenus.com/pdfs/Dysport_Full_Prescribing_Information.pdf
Description
Dysport Prescribing Information

Learn more about this trial

Dysport ® as an Adjunctive Treatment to Bracing in the Management of Adolescent Idiopathic Scoliosis

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