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The role of the intervertebral disc in the progression of adolescent idiopathic scoliosis: a prospective study using magnetic resonance imaging.

The role of the intervertebral disc in the progression of adolescent idiopathic scoliosis: a prospective study using magnetic resonance imaging. - MRI disc in scoliosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON50461
Enrollment
40
Registered
2016-11-24
Start date
2019-12-03
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scoliosis three-dimensional deviation of the spinal axis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

Inclusion criteria

Inclusion criteria: - Patients diagnosed with adolescent idiopathic scoliosis - Presence of right convex main thoracic structural curve, either in Lenke type 1 or 2; - Female gender - Between 10-16 years of age - Cobb*s angle 20-40 degrees

Exclusion criteria

Exclusion criteria: - Skeletal maturity - Presence of any additional spine pathology such as spondylolysis or -listhesis, M. Scheuermann, congenital spinal abnormalities, spinal tumors and spinal trauma - Previous spinal surgery - Neurological symptoms, deficits or pathology - Syndromes associated with disorders of growth - Any contra-indication for MR Imaging

Design outcomes

Primary

MeasureTime frame
Each MR scan will consist of a standard sagittal-only T2W, developed for IVD imaging. The IVDs of the spine between T1 and S1 will be scanned. The different parameters will be measured semi-automatically. The primary study parameters are changes in MRI timing, sensitivity, dynamic range, spatial distribution and morphological changes of the IVD during AIS progression.

Secondary

MeasureTime frame
The secondary parameters are: 1. Correlation of the findings on MR-imaging with patient-reported outcome measurements using the SRS-22 questionnaire

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)