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Precise intervention and intelligent surgical strategy construction based on multimodal analysis of spinal motion

Precise intervention and intelligent surgical strategy construction based on multimodal analysis of spinal motion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036039
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-10-01
Completion date
Unknown
Last updated
2021-06-28

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

Conditions

Low Back Pain

Interventions

Group 1:Non intervention
Group 2:Rehabilitation treatment
Group 3:drug therapy
Group 4:Rehabilitation therapy + drug therapy
Group 5:Traditional surgery
Group 6:Intelligent operation

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Normal population: (1) Aged 18-80 years old; (2) There was no history of spinal injury or surgery; (3) There was no spinal deformity or chronic paravertebral muscle disease; (4) There was no history of malignant tumor, cardiovascular and cerebrovascular diseases and other systemic diseases such as myasthenia gravis; (5) Able to stand and walk independently, willing to cooperate to complete the specified actions; (6) It can be checked for radioactivity. Conservative treatment: (1) Patients with low back pain who did not receive treatment; (2) It can tolerate the action required by the test; (3) No NSAIDs were taken within 10 days; (4) No allergy to celecoxib or any other component in the drug; (5) Agreed to participate in the trial. Surgical treatment: (1) Aged 18-80 years old; (2) Patients with open or minimally invasive X-ray fluoroscopy guidance were allowed to locate the surgical access within the pedicle; (3) Subjects who voluntarily participated and signed informed consent.

Exclusion criteria

Exclusion criteria: Normal population: (1) Other systemic diseases such as diabetes, myasthenia gravis, etc.; (2) Recent fever, or bowel or bladder dysfunction; (3) Unable to cooperate to complete all research steps; (4) Because X-ray may cause damage to the fetus, fertile women who plan pregnancy or suspected pregnancy are not allowed to participate in the test; (5) Radiation tests are not acceptable. Conservative treatment: (1) History of back surgery; (2) Spinal malignant tumor, infection, fracture, cauda equina syndrome or ankylosing spondylitis or other inflammatory diseases; spinal deformity, such as lumbar spondylolisthesis; (3) Other systemic diseases, such as diabetes and kidney disease; (4) Patients who have received lumbar muscle training in the past year; (5) Unable to cooperate to complete all research steps; (6) Patients with active peptic ulcer / bleeding; (7) Severe osteoporosis, hypertension, heart disease. Surgical treatment: (1) Metal allergy, allergic constitution or multiple drug allergy; (2) Women in pregnancy and lactation period; (3) Subjects with coagulation dysfunction; (4) Subjects who failed in the same segment of spinal surgery and needed a second operation; (5) Those who have been participating in clinical trials of other drugs, medical devices, etc. within the past 3 months; (6) The deformity of pedicle of vertebral arch was abnormal; (7) The researchers think it is not suitable to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
VAS;

Countries

China

Contacts

Public ContactLi-Ming Cheng

Shanghai Tongji Hospital

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

Outcome results

None listed

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