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Fluoroscopy Versus Ultrasound Guidance for Sacral Lateral Branch Radiofrequency Ablation

D

Diskapi Teaching and Research Hospital

Status

Completed

Conditions

Back Pain
Sacroiliac Joint Arthritis

Treatments

Procedure: Sacral lateral branch radiofrequency ablation under ultrasound guidance
Procedure: Sacral lateral branch radiofrequency ablation under fluoroscopy guidance

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Sacroiliac joint is a diarthroidal and synovial joint that receives sensory innervatin by the sacral lateral branches ( commonly S1-3, with variable contributions from L5 dorsal ramus and S4 lateral branch). Sacral lateral branch radiofrequency ablation and block techniques are widely used for the management of sacroiliac joint pain. With the increasing use of ultrasound technology in pain medicine, the ultrasound guided approaches gained popularity. To our knowledge, there are no randomized controlled trials comparing the ultrasound and fluoroscopy approaches for sacral lateral branch radiofrequency ablation. This study aims to compare the ultrasound and fluoroscopy guidance techniques for sacral lateral branch radiofrequency ablation.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Low back pain due to sacroiliac joint dysfunction >6 months with a score ≥ 4 on a numeric rating scale.

    • 50% pain relief after prognostic sacral lateral branch block
  • At least 3 positive physical examination maneuvers [ Faber ( flexioni abduction and external rotation), POSH (posteripr shear), REAB ( resisted abduction), Gaenslen's test, Distraction test]

  • Refractory to conservative therapy

Exclusion Criteria: The exclusion criteria were;

  • Uncontrolled psychiatric or neurological illness
  • Sacroiliac joint pain due to other disorders,
  • Lumbar radiculopathy
  • Rheumatological diseases
  • Systemic active infections
  • Malignancies, previous surgery on the affected sacroiliac joint,
  • History of traumatic hip injury,
  • History of bleeding disorders,
  • Platelet values < 150.000 / µl,
  • Sacroiliac joint injection within the preceding 3 months,
  • Allergy to local anesthetics and steroids,
  • Pregnancy, inability to concent, Implanted pacemaker or defibrilator.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Ultrasound guided sacral lateral branch radiofrequency ablation
Experimental group
Description:
Patients in this group will receive sacral lateral branch radiofrequency ablation under ultrasound guidance.
Treatment:
Procedure: Sacral lateral branch radiofrequency ablation under ultrasound guidance
Fluoroscopy guided sacral lateral branch radiofrequency ablation
Active Comparator group
Description:
Patients in this group will receive sacral lateral branch radiofrequency ablation under fluoroscopy guidance.
Treatment:
Procedure: Sacral lateral branch radiofrequency ablation under fluoroscopy guidance

Trial contacts and locations

1

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Central trial contact

Halil C Kose, MD

Data sourced from clinicaltrials.gov

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