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Clinical efficacy and kinematics study of rehabilitation training and coordinated intervention of non-steroidal anti-inflammatory and analgesic drugs in patients with low back pain

Clinical efficacy and kinematics study of rehabilitation training and coordinated intervention of non-steroidal anti-inflammatory and analgesic drugs in patients with low back pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033369
Enrollment
Unknown
Registered
2020-05-29
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-06-01

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

Department of Spinal Surgery, Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The treatment group (1) patients with untreated low back pain; (2) the waist has good function and can withstand the movements required by the test; (3) not taking nsaids within 10 days; (4) no allergy to celecoxib or any other component of the drug; (5) agree to participate in the experiment. The control group (1) no lumbar deformity; (2) no history of lumbar spine injury or chronic spinal muscle disease (3) no chronic lumbar pain; (4) CT examination was followed by 1 imaging specialist and 1 spinal surgery specialist identified no lumbar spine injury or paraspinal muscle disease was exsit.

Exclusion criteria

Exclusion criteria: The treatment group (1) a history of back surgery; (2) spinal malignancy, infection, fracture, cauda equina syndrome or ankylosis; spondylitis or other inflammatory diseases; spinal deformity, such as lumbar spondylolisthesis; (3) other systemic diseases, such as diabetes and kidney disease; (4) patients who had received psoas muscle training in the past year. (5) unable to complete all the research steps; (6) patients with active gastrointestinal ulcer/bleeding; (7) people with severe osteoporosis, high blood pressure and heart disease. The control group (1) other systemic diseases such as diabetes, myasthenia gravis, etc (2) recent fever, or intestinal or bladder dysfunction (3) unable to complete all the research steps; (4) plan to become pregnant or suspect because of possible harm to the fetus caused by X-ray Fertile women who may become pregnant are excluded from the trial; (5) contraindication of mri; (6) do not accept radiation inspection.

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
Total spinal parameter;

Countries

China

Contacts

Public ContactLiMing Cheng

Department of Spinal Surgery, Shanghai Tongji Hospital

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

Outcome results

None listed

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