Skip to content

A multicenter, randomized controlled clinical study on the treatment of lumbar disc herniation with balanced ridge

Clinical treatment of Lumbar Disc Herniation with balanced Ridge Therapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014664
Enrollment
Unknown
Registered
2018-01-28
Start date
2018-02-01
Completion date
Unknown
Last updated
2018-02-05

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

Conditions

prolapse of lumbar intervertebral disc

Interventions

Group 1:Balanced spinal therapy
Group 2:Traction therapy

Sponsors

Affiliated Hospital of Shaanxi University of traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Accord with the diagnostic criteria of lumbar disc herniation; 2. 18-65 years of age; 3. VAS score = 4, = 8; 4. Informed consent and signature of informed consent.

Exclusion criteria

Exclusion criteria: 1. Undiagnosed acute spinal injury or patients with symptoms of myelitis; 2. with liver and kidney, hematopoietic system, endocrine system, cardiovascular system, nervous system and other serious diseases, various fractures, bone tuberculosis, osteomyelitis, bone tumor, severe osteoporosis in the elderly and mentally ill or too weak physique of the patients can't afford massage stimulation; 3. with obvious vertigo symptoms, TCD (transcranial Doppler ultrasound) had obvious abnormal changes; 4. Patients with acute infectious diseases, gastric or duodenal ulcer and acute perforation can not be treated with whole spinal therapy; 5. Patients with severe skin damage or dermatosis in the treatment site; 6. pregnant women, breast-feeding women, pregnancy for more than three months; 7. the past received surgical treatment of lumbar disc herniation or neck trauma, nearly two weeks received RF, minimally invasive, ozone, and other techniques or closed small needle knife therapy; 8. Participants are currently participating in other clinical trials associated with cervical spon.

Design outcomes

Primary

MeasureTime frame
Lumbar arc distance;

Countries

China

Contacts

Public ContactFeng Yang

Affiliated Hospital of Shaanxi University of Traditional Chinese Medicine

yangfengdudu@163.com+86 15809106666

Outcome results

None listed

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