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Randomized controlled study on the treatment of residual low back and leg pain after PLIF surgery for lumbar spinal stenosis with the Bushen huoxue Decoction.

Randomized controlled study on the treatment of residual low back and leg pain after PLIF surgery for lumbar spinal stenosis with the Bushen huoxue Decoction.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075230
Enrollment
Unknown
Registered
2023-08-30
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

lumbar spinal stenosis

Interventions

Treatment group:Bushen huoxue Formula
control group:Bushen huoxue Formula Simulator

Sponsors

Wangjing hospital of CACMS
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? 40 years old = age = 80 years old; ? The patient had lumbar spinal stenosis combined with instability, and all underwent initial lumbar surgery using PLIF. The surgeries were performed by the same group of physicians; ? Relief of lower back and leg pain after lumbar internal fixation surgery; After removing the drainage, there is recurrent low back and leg pain, with a score of 4 = VAS = 7; And postoperative MRI confirmed the presence of intraoperative hematoma. ? The patient meets the diagnostic criteria of both Western medicine and kidney deficiency and blood stasis syndrome after surgery; ? The patient voluntarily participated in this study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: ? Patients with lumbar tuberculosis, lumbar tumors, lumbar compression fractures, or severe osteoporosis; ? Postoperative complications include infection, organ failure, spinal cord and nerve injury, cerebrospinal fluid leakage, loose or broken internal fixation, etc; ? Individuals with severe allergic constitution or allergic to traditional Chinese medicine.

Design outcomes

Primary

MeasureTime frame
Assessment of waist and leg pain;IL-6;

Secondary

MeasureTime frame
Lumbar functional assessment;Postoperative magnetic resonance imaging;

Countries

China

Contacts

Public ContactSun Wu

Wangjing hospital of CACMS

sunwu1978@sina.com+86 136 6138 6553

Outcome results

None listed

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