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Prospective Study of Scheuermann's Kyphosis

Prospective Study of Scheuermann's Kyphosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00738309
Acronym
PSK
Enrollment
147
Registered
2008-08-20
Start date
2006-05-31
Completion date
2013-12-31
Last updated
2016-04-19

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

Conditions

Scheuermann's Kyphosis

Keywords

Treatment Outcomes, Spinal Deformity, Scheuermann's Kyphosis

Brief summary

The purpose of this study to determine the radiographic and clinical outcomes of spinal deformity surgical treatment in patients with Scheuermann's Kyphosis.

Interventions

None listed

Sponsors

DePuy Spine
CollaboratorINDUSTRY
Setting Scoliosis Straight Foundation
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 21 Years
Healthy volunteers
No

Inclusion criteria

* Patient age \< 21 years * Male or female * Diagnosis of classical Scheuermann's Kyphosis (3 successive vertebrae wedged 5 degrees or more, +/- end plate deformities) or idiopathic structural Kyphosis (rigid structural kyphosis without classic Scheuermann's Kyphosis findings). * for which surgical treatment is recommended to prevent progression of the curvature or to correct trunk deformity (unacceptable cosmesis) - any deformity magnitude. OR * for which surgical treatment is not being undertaken (and alternate treatment, i.e. bracing, or observation) is being pursued for any curve magnitude of clinical concerns of Scheuermann's Kyphosis. * Inclusion Criteria for Anterior Release (for those surgeons performing anterior release surgery): Deformity magnitude = any degree and any other criteria defined by the individual surgeon. * Posterior disc herniation is not an

Exclusion criteria

from being in the study, only from being in the Posterior surgery group - these patients will be defaulted to Ant/Post Surgery. * Only patients that have had a pre-op MRI performed as a part of their routine care, should be included in this study.

Design outcomes

Primary

MeasureTime frame
radiographic outcomes2 years

Secondary

MeasureTime frame
Clinical outcomes2 years
Health related quality of life outcomes2 years

Countries

Germany, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026