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Percutaneous Transcatheter Genicular Embolization in Osteoarthritis

Percutaneous Transcatheter Genicular Embolization in Osteoarthritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07361198
Enrollment
20
Registered
2026-01-22
Start date
2026-02-02
Completion date
2029-12-01
Last updated
2026-02-04

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

Conditions

Osteoarthitis, Osteoarthritic Knee Pain, Osteo Arthritis of the Knee

Keywords

genicular artery embolisation, osteoarthritis, MSK embolisation

Brief summary

This clinical study investigates a minimally invasive treatment called percutaneous transcatheter embolization of knee arteries for patients with chronic knee pain caused by advanced knee osteoarthritis or persistent pain after total knee replacement. Osteoarthritis of the knee is a common degenerative condition that can lead to long-term pain, reduced mobility, and decreased quality of life, and some patients do not achieve sufficient relief with standard treatments. The study is based on the hypothesis that targeted embolization of small arteries supplying the inflamed tissues of the knee can safely reduce abnormal blood flow associated with inflammation, leading to pain relief and improved knee function. During the procedure, a thin catheter is guided through the blood vessels to the affected area of the knee, where a temporary embolic agent is administered to reduce pathological blood supply. The aim of the study is to evaluate the safety and effectiveness of this procedure by assessing changes in pain intensity, knee function, and quality of life over a follow-up period of up to 24 months. The results of this study may help determine whether this minimally invasive approach can offer a new treatment option for patients who have limited alternatives for managing chronic knee pain

Detailed description

This is a prospective, single-center, interventional pilot study designed to assess a catheter-based endovascular technique targeting pathological vascular changes associated with chronic knee pain. The intervention focuses on selective embolization of abnormal synovial and periarticular arterial branches identified by angiographic imaging as areas of increased perfusion related to inflammatory activity. The procedure is performed in an angiography suite under local anesthesia. Vascular access is obtained via the common femoral artery, followed by selective catheterization of the arterial branches supplying the knee joint. Digital subtraction angiography is used to visualize hypervascular regions, typically seen as focal contrast enhancement ("blush"). These regions are considered targets for treatment. Embolization is carried out using a temporary embolic suspension administered through a microcatheter until adequate flow reduction in the target vessels is achieved, while preserving normal surrounding circulation. Participants undergo standardized clinical and imaging assessments before the intervention and during scheduled follow-up visits over a two-year period. Follow-up evaluations are intended to capture longitudinal changes in clinical status and to monitor for any procedure-related adverse events. The study emphasizes procedural safety, technical feasibility, and post-interventional monitoring rather than comparison with alternative therapies. Data collected during the study are analyzed using descriptive and paired statistical methods appropriate for an exploratory pilot design. The study is conducted in accordance with applicable ethical standards and regulatory requirements, with particular attention to patient safety, data protection, and transparency of reporting. The findings are expected to provide technical and clinical insights to inform future larger-scale studies and potential integration of this approach into clinical practice.

Interventions

The procedure will be performed in the angiography room under local anesthesia. After puncturing the common femoral artery, a microcatheter will be inserted into the arterial branches supplying the knee joint and DSA will be performed. The target lesions have a typical "blush" appearance representing pathological neovascularization. Embolization will be performed by applying a suspension of Imipenem/Cilastatin dissolved in saline with a contrast agent until flow in the target branch is stopped.

Sponsors

Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 40 to 80 years * Clinical symptoms consistent with chronic knee pain * Radiographically confirmed knee osteoarthritis of Kellgren-Lawrence grade II-IV or persistent knee pain following total knee arthroplasty * Insufficient pain relief after standard conservative treatment (e.g., pharmacological therapy, physical therapy, or injections) * Ability to understand the study procedures and provide written informed consent \_ Willingness and ability to comply with the study procedures and follow-up schedule

Exclusion criteria

* Active local or systemic infection * Known coagulation disorders or ongoing anticoagulation that cannot be safely interrupted * Significant peripheral arterial disease affecting the lower limbs * Known allergy or contraindication to iodinated contrast agents * Severe renal impairment * History of fibromyalgia or other generalized chronic pain syndromes that may confound pain assessment * Pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
VAS (Visual Analog Scale) scoreIn 1st, 3rd, 6th, 12th and 24th month after the procedure.A VAS score for knee pain uses a 0-10 scale, where 0 means no pain, and 10 means the worst imaginable pain, helping quantify intensity, often categorized as mild (1-3), moderate (4-6), and severe (7-10) to assess pain levels or treatment effectiveness.
WOMAC ( Western Ontario and McMaster Universities Osteoarthritis Index) scoreIn 1st, 3rd, 6th, 12th and 24th month after the procedure.The total WOMAC score can range from 0 to 96, with a higher number indicating greater disease severity. The final number is calculated by adding up the points in three separate subscales that assess pain (0-20 points), stiffness (0-8 points), and knee joint function (0-68 points).
KOOS (Knee Injury and Osteoarthritis Outcome Score) scoreIn 1st, 3rd, 6th, 12th and 24th month after the procedure.The KOOS score is a patient-completed questionnaire assessing knee health and function across five areas: Pain, Symptoms (stiffness/swelling), Activities of Daily Living (ADL), Sport \& Recreation, and Quality of Life (QoL). It uses a 0-100 scale (0=worst, 100=best) to track outcomes after knee injuries or arthritis, helping evaluate treatment effectiveness.

Secondary

MeasureTime frameDescription
Analgetics useIn 1st, 3rd, 6th, 12th and 24th month after the procedure.Amount of analgesic use in mg per day

Countries

Czechia

Contacts

CONTACTPatrik Matras, MUDr.
patrik.matras@kzcr.eu+420 604 753 473
CONTACTPavol Viglas
papo.viglas@gmail.com+420 775 733 343

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026