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Clinical Trials/NCT04945343
NCT04945343
Unknown
Not Applicable

Long-Term Follow-Up Of Surgical Management Of Early Onset Scoliosis Using Growing Rods

Assiut University1 site in 1 country30 target enrollmentJune 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Early-Onset Scoliosis Deformity of Spine
Sponsor
Assiut University
Enrollment
30
Locations
1
Primary Endpoint
Percentage of improvement in the functional outcome of these patients using the EOSQ-24, Arabic Version)
Last Updated
4 years ago

Overview

Brief Summary

The aim of this work is to evaluate the long-term outcome of the graduates (those who completed the gradual lengthening procedures), to better understand the full scope and natural course of Growing Rods treatment for EOS and to have a glimpse of what happens to the graduates.

Detailed Description

The management of progressive early onset scoliosis (EOS) is challenging. The natural history can be severe deformity, restrictive lung disease, and early mortality . In the past, the standard of care for these children was early definitive spinal fusion and instrumentation. The belief was that a short and straight spine was superior to a long and deformed spine despite the negative effects of a short trunk. The principles of EOS treatment have changed with the appreciation that early fusion of the thoracic spine limits the growth of the spine and lungs, and eventually leads to respiratory failure and increased mortality. Furthermore, the cosmetic disfigurement from the disproportionate Trunk-Limb length is always not acceptable by the patients. The surgical treatment strategy for EOS has evolved significantly with the use of modern growth friendly implants, of these, Growing Rods(GR), first described by Moe and colleagues, attempt to allow the growth of the spine and thorax while controlling curve progression to preserve normal lung volume. Since then, several modifications and developments have been made and introduced worldwide. Evaluation of the mid to long-term follow up has seldom been reported in the literature. In Assiut university hospital the investigators operated a fair amount of children with EOS using growing rods starting 2009, with favourable short term results. The long-term outcome of the graduates (those who completed the gradual lengthening procedures), remains yet to be evaluated and reported. Research Methods and techniques: Type of the study: case series Study Setting: Assiut University Hospitals, Department of Orthopaedics, Spine Surgery Unit. Study subjects: 1. Inclusion criteria: Any patient with EOS who has been managed with GRs in our centre. 2. Exclusion criteria: Patients whose parents or guardians are not willing to participate in the study. 3. Sample Size Calculation: All patients with EOS operated in our centre who have completed the GR procedures and became graduates since we started doing surgeries in 2009 to the present date. We expect to have complete data for 30 patients during the study period. -Study tools (in detail, e.g., lab methods, instruments, steps, chemicals, ): * Data sheet (Personal data, Cobb's angle, kyphosis angle, Shoulder balance, Coronal and sagittal balance, Pelvic obliquity, T1-S1 height,Span-Height ratio, patient satisfaction score (Likert scale). * Early Onset Scoliosis 24-Item Questionnaire (EOSQ-24) Arabic version . * Radiological assessment (Cobb's angle, kyphosis angle, Shoulder balance, Coronal and sagittal balance, Pelvic obliquity, T1-S1 height, Implant Failure.) * All data will be collected and recorded using the REDCap to facilitate data recording, analysis and creation of safe dedicated database. Research outcome measures: 1. Primary (main): Percentage of improvement in the functional outcome of these patients using the EOSQ-24, Arabic Version) 2. Secondary (subsidiary): 1-Patient satisfaction (Likert scale). 2 Trunk Height Gain (T1-S1 height). 3-Span-Height ratio. 4-The degree of correction of the scoliosis and kyphosis. 5-Maintenance of sagittal and coronal balance. Incidence of complications (PJK, DJK, recurrent infections, neurology, crankshaft phenomenon, etc)

Registry
clinicaltrials.gov
Start Date
June 2021
End Date
June 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amr Hatem Ahmed Mohammed

Assistant lecturer

Assiut University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Patients whose parents or guardians are not willing to participate in the study.

Outcomes

Primary Outcomes

Percentage of improvement in the functional outcome of these patients using the EOSQ-24, Arabic Version)

Time Frame: Through study completion, an average of 2 years.

A score that measures the wider dimensions of outcomes involving the quality of life of patients and caregivers post-treatment.

Secondary Outcomes

  • Patient satisfaction (Likert scale)(Through study completion, an average of 2 years.)
  • The degree of correction of the scoliosis and kyphosis.(Through study completion, an average of 2 years.)
  • Trunk Height Gain (T1-S1 height).(Through study completion, an average of 2 years.)
  • sagittal and coronal balance(Through study completion, an average of 2 years.)

Study Sites (1)

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