Skip to content

Mechanism of Prone Traction-Thrust Manipulation on LDH Radicular Pain Based on Multimodal Data

Mechanism of Prone Traction-Shaking and Thrusting Manipulation in Treating Lumbar Disc Herniation Radicular Pain: A Multimodal Data-Based Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001504
Enrollment
Unknown
Registered
2026-06-17
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Lumbar Disc Herniation (LDH) Radicular Pain

Interventions

Tractive Vibration Thrust Group:Prone Tractive Vibration Thrust Manipulation plus Basic Care (bed rest, lumbar brace, acupuncture, and optional Celecoxib/Eperisone for acute pain)
Conventional Massage Group (Supplementary):Conventional Massage plus Basic Care (bed rest, lumbar brace, acupuncture, and optional Celecoxib/Eperisone for acute pain)

Sponsors

Guangdong Second Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1)Meet the diagnostic criteria for lumbar disc herniation (LDH) according to the Clinical Diagnosis and Treatment Guidelines - Orthopedics Volume (Chinese Medical Association, 2009) and the Diagnostic Efficacy Criteria for Traditional Chinese Medicine Diseases - Lumbar Disc Herniation Diagnostic Criteria (State Administration of Traditional Chinese Medicine, 1994), with associated radicular pain; 2)Right-handed; 3)Aged between 25 and 60 years; 4)Disease duration = 3 months and Visual Analog Scale (VAS) score = 4; 5)No pain in other areas except that caused by LDH; 6)No regular treatment received within 3 months prior to enrollment; 7)Volunteer to participate in this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Patients with clinical manifestations predominantly characterized by soreness, distension, or numbness rather than pain as the primary symptom, or pain caused by other diseases; 2) Patients complicated with urinary/fecal incontinence or foot drop; 3) Patients with extremely severe clinical symptoms requiring surgical treatment; 4) Contraindications to MRI examination (e.g., metal implants, claustrophobia, etc.); 5) Long-term use of analgesics, history of smoking or alcohol addiction; 6) Complicated with severe primary diseases of the digestive system, cardiovascular system (such as hypertension, coronary heart disease), hematopoietic system, or mental disorders; women who are lactating or pregnant; 7) Complicated with vertebral fractures, spinal cord tumors, or compression symptoms caused by factors other than lumbar disc herniation; 8) Poor compliance, inability to return for follow-up visits, inability to undergo MRI examination, or incomplete imaging data.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS) Score;Japanese Orthopaedic Association (JOA) Low Back Pain Score;Oswestry Disability Index (ODI);Biomechanical Parameters Measured by the DIERS formetric 3D System;Morphological Parameters of Nerve Root and Intervertebral Disc Measured by MRI;

Secondary

MeasureTime frame
Straight Leg Raise (SLR) Angle;Excellent and Good Rate of Therapeutic Effect;

Countries

China

Contacts

Public ContactZhang Yanming

Guangdong Second Traditional Chinese Medicine Hospital

867614345@qq.com13580463985

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026