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Multicenter study on intelligent surgical intervention strategy for low back pain based on whole spine imaging and posture analysis technology

Multicenter study on intelligent surgical intervention strategy for low back pain based on whole spine imaging and posture analysis technology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030820
Enrollment
Unknown
Registered
2020-03-15
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-03-16

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

Conditions

Low back pain

Interventions

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Drug therapy combined with rehabilitation training group: 1. Untreated patients with low back pain; 2. The lumbar function is good and can withstand the actions required by the test. 3. Able to cooperate in completing all research steps; 4. Agree to participate in the test. Simple rehabilitation training group: 1. Untreated patients with low back pain; 2. The lumbar function is good and can withstand the actions required by the test; 3. Able to cooperate in completing all research steps; 4. Agree to participate in the test. Normal group: 1. After CT examination, one imaging expert and one spinal surgery expert confirmed that there was no lumbar spine injury or paraspinal muscle disease; 2. Able to cooperate in completing all research steps; 3. Patients who can't be radiographed.

Exclusion criteria

Exclusion criteria: Drug therapy combined with rehabilitation training group: 1. Has a history of back surgery; 2. With spinal malignant tumor, infection, fracture, cauda equina syndrome or ankylosing spondylitis or other inflammatory diseases; Spinal deformity, such as lumbar spondylolisthesis; 3. With other systemic diseases, such as diabetes and kidney diseases; 4. Patients who have received lumbar muscle training in the past year; 5. Taking NSAIDs within 10 days; 6. Allergy to celecoxib or any other component in the drug; 7. Sulfanilamide allergy; 8. Patients with active peptic ulcer/hemorrhage; 9. With severe osteoporosis, hypertension and heart disease. Simple rehabilitation training group: 1. With history of back surgery; 2. With spinal malignant tumor, infection, fracture, cauda equina syndrome or ankylosing spondylitis or other inflammatory diseases; Spinal deformity, such as lumbar spondylolisthesis; 3. With other systemic diseases, such as diabetes and kidney diseases; 4. Patients who have received lumbar muscle training in the past year; 5. Taking NSAIDs within 10 days; 6. With severe osteoporosis, hypertension and heart disease. Normal group: 1. With other systemic diseases such as diabetes, myasthenia gravis, etc.; 2. Patients with recent fever or intestinal or bladder dysfunction; 3. Women of childbearing ability who has planned or suspected pregnancy due to possible harm to the fetus caused by X-rays; 4. Patients with contraindications of MRI; 5. With lumbar deformity; 6. With history of lumbar spine injury or chronic diseases of paraspinal muscles 7. With chronic lumbar pain.

Design outcomes

Primary

MeasureTime frame
Global spine parameters;

Countries

China

Contacts

Public ContactCheng Liming

Department of Spine Surgery, Tongji Hospital

limingcheng@tongji.edu.cn+86 21-66111706

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026