Correlation Among Standing-sitting Sagittal Spinal Alignment, Paravertebral Muscle and Postoperative Clinical Outcomes in Patients With Adult Degenerative Scoliosis

December 24, 2020 updated by: Peking University Third Hospital
This is a prospective single-center study. Patients with adult degenerative scoliosis are prospectively enrolled and followed. All patients will take standard standing and sitting posteroanterior and lateral whole spine X-ray and lumbar MRI examination before and after surgery. Functional evaluation and radiographs were assessed preoperatively and postoperatively.This study will focus on the correlation among standing-sitting sagittal spinal alignment, paravertebral muscle and postoperative clinical outcomes in patients with adult degenerative scoliosis.

Study Overview

Detailed Description

The sagittal alignment of the spine, or sagittal balance, describe the ideal and normal sagittal spinal curvature distribution. With the deepening of the research on spinal morphology, function and pathology, more and more researchers pay attention to the role of sagittal alignment in the diagnosis and treatment of spinal deformity diseases. Some studies have shown that the restoration of patients with appropriate sagittal alignment can significantly improve their quality of life. Besides, paravertebral muscle can also influence the retaining of sagittal alignment. However, how to define the ideal sagittal alignment is still controversial for different patients with adult degenerative scoliosis(ADS) .

It was proved that the differences in sagittal parameters of the standing and sitting positions positions were influenced by age, gender and pelvic incidence(PI). In addition, patients with high PI are more prone to sagittal decompensation after long segment fixation (fixation of three or more segments) .Therefore, We speculate that the sagittal curvature of patients with large PI changes greatly from standing position to sitting position. So after long segment fixation, the spine in the state of standing position is more difficult to adapt to the changes of curvature and stress in sitting position, which is the possible reason that patients with high PI are more prone to sagittal decompensation. At present, how to design the proper corrective goals for patients according to both sagittal alignment and paravertebral muscle needs further research.

Thus, this study is aim to explore these three points about ADS patients: the characteristics of the sagittal spinal alignment changes from standing to sitting ; the adaption of the spine curvature in the standing and sitting position after long segment fixation surgery and the relationship among standing-sitting sagittal spinal alignment, paravertebral muscle and postoperative clinical outcomes.

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Beijing
      • Beijing, Beijing, China, 100191
        • Peking University Third Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

45 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with adult degenerative scoliosis who will undergo corrective surgery in Peking university third hospital.

Description

Inclusion Criteria:

  • Clinical diagnosis of adult degenerative scoliosis
  • Cobb angle ≥10°

Exclusion Criteria:

  • Neuromuscular diseases
  • Arthritis
  • Tumor
  • A previous history of lumbar fusion surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients with degenerative scoliosis
Routine examination

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The sagittal spinal parameters in degrees
Time Frame: 3 months after surgery
The 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) Cobb angle of the curves
3 months after surgery
The sagittal spinal parameters in degrees
Time Frame: 6 months after surgery
The 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) Cobb angle of the curves
6 months after surgery
The sagittal spinal parameters in degrees
Time Frame: 12 months after surgery
The 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) Cobb angle of the curves
12 months after surgery
The sagittal spinal parameters in millimeters
Time Frame: 3 months after surgery
SVA (sagittal vertical axis, The offset between the center of C7 and the plumb line drawn from posterosuperior corner of S1)
3 months after surgery
The sagittal spinal parameters in millimeters
Time Frame: 6 months after surgery
SVA (sagittal vertical axis, The offset between the center of C7 and the plumb line drawn from posterosuperior corner of S1)
6 months after surgery
The sagittal spinal parameters in millimeters
Time Frame: 12 months after surgery
SVA (sagittal vertical axis, The offset between the center of C7 and the plumb line drawn from posterosuperior corner of S1)
12 months after surgery
parameters of paraspinal muscles
Time Frame: 12 months after surgery
the cross-sectional area (square centimeter)
12 months after surgery
parameters of paraspinal muscles
Time Frame: 12 months after surgery
fatty infiltration rate of paraspinal muscles
12 months after surgery
functional outcomes of paraspinal muscles
Time Frame: 3 months after surgery
the time of paraspinal muscle strength test
3 months after surgery
functional outcomes of paraspinal muscles
Time Frame: 6 months after surgery
the time of paraspinal muscle strength test
6 months after surgery
functional outcomes of paraspinal muscles
Time Frame: 12 months after surgery
the time of paraspinal muscle strength test
12 months after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Disability assessed by the Oswestry Disability Index (ODI)
Time Frame: 3 months after surgery; 6 months after surgery; 12 months after surgery;
The Oswestry Disability Index (ODI) (0-100) is used to assess disability.Higher scores mean a worse outcome.
3 months after surgery; 6 months after surgery; 12 months after surgery;
Disability assessed by the Japanese Orthopaedic Association (JOA)
Time Frame: 3 months after surgery; 6 months after surgery; 12 months after surgery;
Japanese Orthopaedic Association (JOA)(-6-29) Scores is used to assess disability.Higher scores mean a better outcome.
3 months after surgery; 6 months after surgery; 12 months after surgery;
Back pain assessed by the VAS
Time Frame: 3 months after surgery; 6 months after surgery; 12 months after surgery;
The Visual Analog Scale (0-10) is used to evaluate back pain.Higher scores mean a worse outcome.
3 months after surgery; 6 months after surgery; 12 months after surgery;
Leg pain assessed by the VAS
Time Frame: 3 months after surgery; 6 months after surgery; 12 months after surgery;
The Visual Analog Scale (0-10) is used to evaluate leg pain.Higher scores mean a worse outcome.
3 months after surgery; 6 months after surgery; 12 months after surgery;

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

January 20, 2021

Primary Completion (Anticipated)

December 1, 2021

Study Completion (Anticipated)

January 1, 2024

Study Registration Dates

First Submitted

December 18, 2020

First Submitted That Met QC Criteria

December 24, 2020

First Posted (Actual)

December 30, 2020

Study Record Updates

Last Update Posted (Actual)

December 30, 2020

Last Update Submitted That Met QC Criteria

December 24, 2020

Last Verified

December 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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