Prospective, Multi-Center Adult Spinal Deformity Outcomes Database Registry

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00738439

Acronym

PON

Enrollment

1999

Registered

2008-08-20

Start date

2008-10-01

Completion date

2026-12-01

Last updated

2026-03-27

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

Conditions

Spinal Deformity

Keywords

scoliosis, kyphosis, treatment outcomes, spinal deformity

Brief summary

The clinical, radiographic, and HRQL outcomes will be compared in operative and nonoperative adult spinal deformity patients.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Diagnosis of adult degenerative or idiopathic scoliosis with a curvature of the spine measuring greater than or equal to 20 degrees * Sagittal Vertical Axis (SVA) \> 5cm * Pelvic Tilt \> 25 degrees * Thoracic kyphosis \> 60 degrees * Age 18 or greater at the time of enrollment.

Exclusion criteria

* Diagnosis of scoliosis other than degenerative or idiopathic (i.e. paralytic/neuromuscular, congenital) * Age \<18 yrs at time of surgery or initial consultation

Design outcomes

Primary

Measure	Time frame	Description
Radiographic	initial visit, 1 year, 2 years, 3-5 years	Coronal and Sagittal views of the spine

Secondary

Measure	Time frame	Description
Clinical outcomes	initial visit, 1 year, 2 years, 3-5 years	physical examination/pain scale
Health related quality of life	initial visit, 1 year, 2 years, 3-5 years	Oswestry, SRS22r, SF-36, LSDI, EQ5D3L, NDI DRAM (optional)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORShay Bess, MD

Denver International Spine Center

Outcome results