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Investigating the Effect of Genicular Artery Embolization for the Treatment of Knee Osteoarthritis Pain

Investigating the Effect of Genicular Artery Embolization for the Treatment of Knee Pain Secondary to Osteoarthritis in patients refferd to Urmia Imam Khomeini Hospital

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240615062136N1
Enrollment
23
Registered
2024-10-18
Start date
2024-09-05
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Osteoarthritis of Knee. Osteoarthritis of knee

Interventions

Intervention group: Patients who undergo embolization of the genicular artery of one knee. Both knees of each patient are examined, and the knees are randomly assigned to either intervention or contro

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age between 45 and 75 years with symptoms of knee pain in both knees Radiographic findings in both knees with a grade of 2 to 4 based on the Kellgren-Lawrence classification VAS score above 50/100 for both knees Pain resistant to medical and supportive treatments for a duration of 3 months All patients must agree not to use any oral or injectable painkillers and supplements during the study period and, if necessary, take medications according to the study protocol

Exclusion criteria

Exclusion criteria: Pregnancy GFR 40 kg/m² History of joint injection in the last 3 months Joint infection or inflammatory joint disease Life expectancy of less than 2.5 years Platelet count less than 30,000 per microliter Allergy to iodinated contrast agents Presence of joint prosthesis or history of joint surgery Absence of palpable pulse

Design outcomes

Primary

MeasureTime frame
Pain Score. Timepoint: Before, after one month and three months of the intervention. Method of measurement: Visual Analogue Scale.;Functional Performance. Timepoint: Before, after one month and three months of the intervention. Method of measurement: The Western Ontario and McMaster Universities Osteoarthritis Index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Noorabadi

Oroumia University of Medical Sciences

noorabadi.par@umsu.ac.ir+98 44 3345 7286

Outcome results

None listed

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