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Analysis of the Application Effect of Integrated Traditional Chinese and Western Medicine Rehabilitation Self-Management in Patients Undergoing Posterior Lumbar Fusion Surgery

Analysis of the Application Effect of Integrated Traditional Chinese and Western Medicine Rehabilitation Self-Management in Patients Undergoing Posterior Lumbar Fusion Surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124924
Enrollment
Unknown
Registered
2026-05-19
Start date
2026-01-16
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

lumbar degenerative diseases, LDD

Interventions

Control Group:none
Integrated traditional Chinese and western medicine rehabilitation self-management Group:none

Sponsors

Wuhan Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine (The Affiliated Hospital of Wuhan Sports University)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with LDD, including lumbar spondylolisthesis (LS) and lumbar spinal stenosis (LSS), with or without intervertebral disc herniation or degenerative lumbar scoliosis, whose radiographic findings (X-ray, computed tomography (CT), and magnetic resonance imaging (MRI)) were consistent with clinical symptoms and signs; 2. Patients with persistent neurological symptoms or typical intermittent claudication; 3. Symptoms did not resolve or worsened after at least 3 months of systematic conservative treatment; 4. Patients who underwent posterior lumbar fusion surgery (Posterior Lumbar Interbody Fusion(PLIF), Transforaminal Lumbar Interbody Fusion(TLIF), Percutaneous Endoscopic Posterior Lumbar Interbody Fusion(PE-PLIF)); 5. Patients with complete perioperative and at least 1-year postoperative follow-up data.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiac, cerebral, renal, or other diseases precluding tolerance to surgery; 2. History of previous lumbar surgery; 3. Presence of severe osteoporosis; 4. Presence of lumbar tumors, tuberculosis, or infectious lesions; 5. Patients with psychological or mental disorders; 6. Incomplete medical records.

Design outcomes

Primary

MeasureTime frame
VAS for low back and leg pain;JOA scores;

Secondary

MeasureTime frame
readmission rate for lumbar issues and reoperation rate during follow-up;postoperative length of hospital stay;postoperative complications;Postoperative first ambulation time;

Countries

China

Contacts

Public ContactTang Jin

Wuhan Orthopaedics Hospital of Integrated Traditional Chinese and Western Medicine (The Affiliated Hospital of Wuhan Sports University)

tangjin725@126.com+86 27 87740941

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026