Lumbar Disc Herniation
Conditions
Interventions
Control Group A (Blank Control Group):Routine Admission Care and Routine Rehabilitation Guidance for Lumbar Disc Herniation During the Perioperative Period
Control Group B (Positive Control Group):In control group A, routine care was combined with postoperative systematized McKenzie therapy.
Experimental group:Based on the intervention of control group B, combined with a whole-cycle Chinese medicine-appropriate techniques-based care plan under the enhanced recovery after surgery (ERAS) co
Sponsors
Jiangxi University of Traditional Chinese Medicine Affiliated Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Participants must meet the following criteria: 1. Diagnosed with lumbar disc herniation according to Western medical diagnostic criteria (ICD-10 code: M51.2) and have undergone lumbar minimally invasive surgery (percutaneous endoscopic discectomy or minimally invasive transforaminal lumbar interbody fusion) at this hospital; 2. Aged 18 to 75 years, with no restriction on gender; 3. Conscious and with normal cognitive function, able to cooperate with the intervention, complete the questionnaire assessments, and undergo the entire follow-up process; 4. Voluntarily participate in this study and have signed a written informed consent form.
Exclusion criteria
Exclusion criteria: Those with combined lumbar spondylolisthesis, lumbar spinal stenosis, spinal deformities, spinal tumors, spinal infections, vertebral fractures, or other lumbar disorders; Those with a history of previous lumbar surgery; Those with severe dysfunction of important organs such as heart, liver, kidney, or hematopoietic system, coagulation disorders, mental illness, or malignant tumors; Those with contraindications foroperations such as skin ulcers, alcohol allergies, fear of needles, or contraindications for moxibustion/ acupuncture; Those currently participating in other similar clinical trials; Those deemed by researchers to be unable to cooperate with the study or at risk of being lost to follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lumbar Spine Dysfunction Index Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain Numerical Rating Scale Score;Japanese Orthopedic Association Lumbar Function Score;Levels of inflammatory markers in trauma;Postoperative complication rate;Rehabilitation Nursing Compliance Assessment;Gastrointestinal Symptoms Assessment Scale Scoring;36-Item Short Form Health Survey (SF-36) Scoring; | — |
Countries
China
Contacts
Public ContactLiu Li-fang
Jiangxi University of Traditional Chinese Medicine Affiliated Hospital
Outcome results
None listed