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The Standing and Sitting Spino-pelvic Sagittal Alignment in Chinese Population

The Standing and Sitting Spino-pelvic Sagittal Alignment in Chinese Population

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04958590
Enrollment
216
Registered
2021-07-12
Start date
2019-02-20
Completion date
2020-03-01
Last updated
2021-07-12

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

Conditions

Sagittal Alignment

Keywords

sagittal alignment, sitting, spinal fusion

Brief summary

This study is aimed to demonstrate the standing and sitting spino-pelvic sagittal alignment in Chinese population, then to explore the influence of spinal fusion on the changes when moving from standing to sitting positon.

Interventions

RADIATIONwhole spine X-ray

Group 1 underwent whole spine X-ray in standing and sitting positions.

Sponsors

Peking University Third Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
42 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

Group 1 90 Healthy Volunteers - age \>40 years, no history of neck pain, back pain, or radicular pain in the previous six months, no history of chronic neck or back pain lasting more than three months, no history of spinal disease or surgery, no spinal deformity or lumbar spondylolisthesis, no history of hip or knee arthroplasty or other realignment surgery of the lower extremities, and no history of neuromuscular disorders. Group 2 126 patients Clinical diagnosis of Lumbar degenerative disease

Exclusion criteria

Group 1 90 Healthy Volunteers \- pregnant Group 2 126 patients * Neuromuscular diseases * Arthritis * Tumor * A previous history of lumbar fusion surgery

Design outcomes

Primary

MeasureTime frameDescription
Group 2 The sagittal spinal parameters in degrees3 months after surgeryThe parameters included TPA (T1 pelvic angle,the angle between the line from the axis of the femoral head to the center of T1 and the line from the axis of the femoral head to the midpoint of the S1 endplate), lumbar lordosis (LL,the angle between the upper endplate of L1 and S1), thoracic kyphosis (TK,The angle between the upper endplate of T4 and the lower endplate of T12), pelvic incidence (PI,The angle between the line perpendicular to the midpoint of the sacral plate and the line connecting this to the midpoint of the hip axis), pelvic tilt (PT,The angle between the line from the middle of the sacral plate to the middle of the hip axis and the vertical line), sacral slope (SS,The angle between the sacral endplate and the horizontal line)
Group 1 The sagittal spinal parameters in degrees6 months after study startedThe parameters included TPA (T1 pelvic angle,the angle between the line from the axis of the femoral head to the center of T1 and the line from the axis of the femoral head to the midpoint of the S1 endplate), lumbar lordosis (LL,the angle between the upper endplate of L1 and S1), thoracic kyphosis (TK,The angle between the upper endplate of T4 and the lower endplate of T12), pelvic incidence (PI,The angle between the line perpendicular to the midpoint of the sacral plate and the line connecting this to the midpoint of the hip axis), pelvic tilt (PT,The angle between the line from the middle of the sacral plate to the middle of the hip axis and the vertical line), sacral slope (SS,The angle between the sacral endplate and the horizontal line)
Group 1 The sagittal spinal parameters in millimeter6 months after study startedSVA (sagittal vertical axis, The offset between the center of C7 and the plumb line drawn from posterosuperior corner of S1)

Secondary

MeasureTime frameDescription
Group 2 Disability assessed by the Oswestry Disability Index (ODI)3 months after surgeryThe Oswestry Disability Index (ODI) (0-100) is used to assess disability.Higher scores mean a worse outcome.
Group 2 Back pain assessed by the VAS3 months after surgeryThe Visual Analog Scale (0-10) is used to evaluate back pain.Higher scores mean a worse outcome
Group 2 Leg pain assessed by the VAS3 months after surgeryThe Visual Analog Scale (0-10) is used to evaluate leg pain.Higher scores mean a worse outcome.

Countries

China

Outcome results

None listed

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