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Comparison of Conventional and Cooled Radiofrequency Ablation in Knee Osteoarthritis

G

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Status

Enrolling

Conditions

Knee Osteoarthritis

Treatments

Device: Radiofrequency ablation

Study type

Interventional

Funder types

Other

Identifiers

NCT06863181
AEŞH-EK-2025-064

Details and patient eligibility

About

The aim of this study was to examine and compare the effects of conventional and cooled radiofrequency ablation on pain and disability levels in patients with knee pain resistant to other treatments due to knee osteoarthritis.

Enrollment

26 estimated patients

Sex

All

Ages

50 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Knee pain lasting more than 6 months

  • Age between 50 and 80

  • Diagnosis of radiographically proven grade III or IV knee osteoarthritis according to the Kellgren-Lawrence Grading Scale, marked narrowing of the medial compartment of the tibiofemoral joint space

  • Presence of pain resistant to conservative treatment

    • Exercise
    • Physical therapy agents
    • Use of oral anti-inflammatory agents

Exclusion criteria

  • History of trauma to the knee area
  • History of knee surgery
  • Presence of systemic inflammatory disease affecting the knee joint
  • Presence of peripheral neuropathy or radiculopathy
  • Pregnancy
  • Hemodynamic instability
  • Presence of skin or soft tissue infection at the injection site
  • Refusal to participate in the study
  • Presence of acute knee pain with accompanying inflammatory findings
  • Presence of a serious psychiatric disorder or neurological disease Having received an intra-articular injection within the last 3 months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

26 participants in 2 patient groups

Conventional Radiofrequency Ablation
Active Comparator group
Description:
Conventional radiofrequency ablation with fluoroscopy
Treatment:
Device: Radiofrequency ablation
Cooled Radiofrequency Ablation
Experimental group
Description:
Cooled radiofrequency ablation with ultrasound
Treatment:
Device: Radiofrequency ablation

Trial contacts and locations

1

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Central trial contact

Ayşe Naz Kalem Özgen, Specialist

Data sourced from clinicaltrials.gov

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