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Ultrasound-guided Botulinum Toxin A Injection in Patients with failed back surgery syndrome

Ultrasound-guided Botulinum Toxin A Injection in Patients with Failed Back Surgery Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020336
Enrollment
Unknown
Registered
2018-12-24
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Failed Back Surgery Syndrome

Interventions

Internal heat needle therapy group:Internal heat needle therapy
Botulinum toxin A injection therapy:Botulinum toxin A injection

Sponsors

Foshan Chancheng District Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: With the approval of the Medical Ethics Committee of the Hospital, FBSS patients were selected from June 2018 to June 2019 in Chancheng District Central Hospital of Foshan City. The clinical diagnostic criteria of FBSS are as follows: 1. After laminectomy or nucleus pulposus removal, lumbar, hip pain, radiation stubborn pain or other discomfort symptoms still exist in patients with lumbar disc protrusion; 2. Examination showed corresponding spinous processes and paravertebral tenderness, positive straight leg elevation and reinforcement test on the affected side, and abnormal muscle strength, sensation and reflex of the affected lower limbs. Preoperative CT or MRI findings of the lumbar spine suggest corresponding disc herniation; 3. Exclude the lumbago and leg pain caused by tuberculosis, tumors and other factors. Patient's aged from 35 to 80 years old, regardless of gender. All patients underwent spinal internal fixation to remove the intervertebral disc at the stage of lesion, and after operation, lumbar discomfort, limb pain or numbness occurred.

Exclusion criteria

Exclusion criteria: Patients with pathological changes in the spinal canal were excluded by MRI reexamination, patients with pain caused by residual disc or bone debris falling into the spinal canal after lumbar surgery, patients with osteogenic spinal stenosis, calcification of intervertebral disc and cauda equina syndrome were excluded, patients with secondary infection after lumbar surgery were excluded, and patients who were reluctant to receive silver needle therapy because of fear of pain were excluded. Patients with severe cardiovascular and cerebrovascular diseases were excluded; diabetic patients with uncontrolled blood sugar were excluded; patients with lumbar or sacral tumors or tuberculosis will be excluded; patients with abnormal coagulation function were excluded.

Design outcomes

Primary

MeasureTime frame
M-JOA Scale;

Countries

China

Contacts

Public ContactZhipeng Li

Central Hospital of Foshan, Chancheng District

545076940@qq.com+86 13711271347

Outcome results

None listed

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