Skip to content

Clinical study of Sun's seesaw tendon management in the treatment of lumbar intervertebral disc herniation

Clinical study of Sun's seesaw tendon management in the treatment of lumbar intervertebral disc herniation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085249
Enrollment
Unknown
Registered
2024-06-04
Start date
2024-06-04
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Lumbar Disc Herniation

Interventions

Experimental group:The patient is prone and treated with the first eight routines of the nine-style sixteen-foot method, and then focuses on the Huatuo chiropractic points on both sides of the lumbar
Control group:Hold the crossbar of the seesaw bed with both hands, control the power of the pedaling, and use the heel part to carry out vertical compression on the 1~2cm on both sides of the L3, L4,

Sponsors

Institute of Chinese Medical History Documents, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients diagnosed with lumbar intervertebral disc herniation; (2) 18 years old= age = 65 years old; (3) Subjects voluntarily participate and sign the informed consent form; (4) Mild or moderate herniation of L3/L4, L4/L5, L5/S1 intervertebral disc confirmed by CT or MRI, with the protrusion not exceeding 5mm or the protrusion compressing the dural sac not exceeding 30%; (5) The patient had no clear indication for surgery and chose conservative treatment.

Exclusion criteria

Exclusion criteria: (1) Patients with cauda equina syndrome, spinal fracture, bone tuberculosis, ligamentum flavum hypertrophy, dry sciatica, piriformis injury syndrome, dislocation, lumbar spondylolisthesis, severe osteoporosis, calcification, severe adhesion between protrusions and nerve roots, lumbar spinal stenosis and other diseases; (2) Pregnant and lactating females; (3) Complications of hematopoietic system diseases with bleeding tendency, tumors, serious diseases of heart, brain, liver, kidney, blood system and other important organs; Patients with mental and psychological diseases such as cognitive or psychiatric disorders; (4) Patients with rheumatoid and rheumatoid arthritis; (5) Skin damage and trauma on the lower back; (6) Other circumstances judged by the investigator to be inappropriate to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Japanese Orthopaedic Association Scores;

Secondary

MeasureTime frame
visual analogue scale;

Countries

China

Contacts

Public ContactJianfeng Liu

Institute of Chinese Medical History Documents, China Academy of Chinese Medical Sciences

doctor_ljf@hotmail.com+86 186 1152 7911

Outcome results

None listed

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