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Clinical study of wearable lumbar traction device combined with manipulation in the treatment of lumbar disc herniation

Clinical study of wearable lumbar traction device combined with manipulation in the treatment of lumbar disc herniation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006806
Enrollment
Unknown
Registered
2022-11-21
Start date
2022-11-11
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

protrusion of lumbar intervertebral disc

Interventions

control group:Routine lumbar traction and manipulation treatment
test group:Wearable lumbar traction device and manipulation therapy

Sponsors

Yueyang Integrated Chinese and Western Medicine Hospital affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. It met the diagnostic criteria of traditional Chinese and Western medicine for lumbar disc herniation, mainly with lumbar or lumbar leg pain, 8=VAS score =4; 2. Age =20 years and =70 years, both sexes; 3. Indications that meet non-surgical indications; 4. Volunteer to participate in this study and sign the informed consent form. 5 Patients who did not receive medication, manipulation or traction treatment within 2 weeks before enrollment

Exclusion criteria

Exclusion criteria: 1 Patients with neoplasms, tuberculosis, spinal osteomyelitis, spinal fractures, Cauda equina syndrome, ankylosing spondylitis; 2. Non-discogenic causes (such as spinal stenosis, inflammation, tumor, etc.), patients with non-specific low back pain, patients with acute low back pain; 3. Patients with serious cardio-cerebrovascular, liver, kidney and other serious life-threatening primary diseases and psychiatric patients; 4 Pregnant or lactating women; 5. Patients with communication disorders and mental illness 6 Patients with osteoporosis and other diseases

Design outcomes

Primary

MeasureTime frame
Efficient;

Secondary

MeasureTime frame
Likert Rating;the Oswestry Disability Index;Safety Evaluation;range of motion;visual analogue scale;

Countries

China

Contacts

Public ContactZhang Hong
zhanghongdoctor@sina.com18930566930

Outcome results

None listed

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