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Fluoroscopy-Guided Bipolar Radiofrequency Thermocoagulation Treatment for Discogenic Low Back Pain

Fluoroscopy-Guided Bipolar Radiofrequency Thermocoagulation Treatment for Discogenic Low Back Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15006556
Enrollment
Unknown
Registered
2015-06-12
Start date
2015-06-12
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

discogenic pain

Interventions

BRF:bipolar radiofrequency

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: All patients presented with LBP with or without pseudo-radicular referral for at least 6 months. Additionally, all patients exhibited the following criteria: 1. a lack of satisfactory improvement after adequate conservative therapy; 2. concordant pain upon provocative discography in the affected disc, but not in the control discs; 3. LBP exacerbated by sitting; 4. disc height>50% of the control disc; 5. high-intensity zones (HIZs) in the affected disc detected by MRI scans; 6. single-level disc disease without evidence of additional degenerative changes in other discs; 7. the absence of neural compression lesions; and 8. normal neurological examination findings.

Exclusion criteria

Exclusion criteria: patients with compressive radiculopathy, an extruded or sequestered disc, calcification of the extruded disc, bony spinal canal stenosis, more than 2 symptomatic levels, previous surgery at the symptomatic level, severe scoliosis, spondylolisthesis, spinal tumor, fracture, infection, segmental instability, coagulation dysfunction, serious cardiopulmonary dysfunction, drug abuse, psychological issues by exam or history,beck depression inventory (BDI) > 20 or pregnancy.

Design outcomes

Primary

MeasureTime frame
VAS;Oswestry disability index (ODI) score;

Secondary

MeasureTime frame
Pain relief;reduction of analgesic dose;patient satisfaction;

Countries

China

Contacts

Public ContactYanping Li
yp7391@sina.com+86 13701197818

Outcome results

None listed

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