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RECRUITING

NCT05423587

Genicular Artery Embolisation for Knee Osteoarthritis II

Sponsor: Varian, a Siemens Healthineers Company

View on ClinicalTrials.gov

Summary

This clinical study is designed as a double-blind sham controlled randomised trial with the option of sham group crossover to receive the GAE treatment at 6 months after unblinding. This study will determine if embolisation of abnormal neovasculature arising from branches of the genicular arteries reduces pain in patients with knee osteoarthritis. The study patient population will consist of up to 110 subjects with knee pain for at least 3 months that is resistant to conservative treatment measures. Subjects will be treated with knee embolisation or 2 mL of saline in the sham arm. At 6 months, all subjects in the sham arm will be allowed to cross-over and receive the embolisation procedure with a follow-up duration of 18 months. The total planned study duration is 3.5 years.

Official title: Genicular artEry embolisatioN in patiEnts With oSteoarthrItiS of the Knee II

Key Details

Gender

All

Age Range

45 Years - Any

Study Type

INTERVENTIONAL

Enrollment

110

Start Date

2022-10-30

Completion Date

2028-06-30

Last Updated

2024-12-03

Healthy Volunteers

Conditions

Knee Osteoarthritis

Interventions

PROCEDURE

Genicular Artery Embolisation

Transarterial catheter directed embolisation of hypervascularity in patients with mild to moderate knee osteoarthritis

PROCEDURE

Genicular Artery Injection

Transarterial catheter directed injection of normal (0.9%) saline in patients with mild to moderate knee osteoarthritis

Inclusion Criteria: ALL inclusion criteria below need to be fulfilled for the patient to participate in the study. * Participant is willing and able to give informed consent for participation in the study. * Participants aged 45 years or above. * Grade 1-3 knee OA on X-ray as per Kellgren-Lawrence Grading Scale * Knee pain for at least 3 months resistant to conservative non-surgical treatment (e.g., physiotherapy, steroid injections, weight loss programs, PRP (platelet-rich plasma) injections) * Be able to lie flat for at least 6 hours-this will be assessed by asking how participants sleep (bed, chair recumbent, semi-recumbent) and assessing what prevents them from lying flat overnight (breathlessness, back pain, etc) * Minimum score of 50 on baseline 0 - 100 VAS Exclusion Criteria: The patient may not enter the study if ANY of the following apply: * Rheumatoid arthritis or infectious arthritis * Severe knee OA (grade 4 on x-ray as per Kellgren-Lawrence Grade) * Renal impairment: eGFR \<45. Assessed from medical records or a blood test if required as is part of standard clinical practice when considering a patient for a therapeutic intervention. * Patients with a bleeding diathesis, or other bleeding risk such as patients on warfarin which cannot be stopped easily (e.g., patients with metallic heart valves) assessed by asking the patient and from medical records. Uncorrectable bleeding diathesis: INR\>1.6, Platelets \<50,000 * Requires oxygen on ambulation. Assessed by asking the patient and from medical records. * Low life expectancy (\<1 year) * Communication difficulty due to language barriers * Contraindication to MRI * Known allergies to barium sulfate, 3-aminopropyltrialkoxysilane, polyphosphazene or IV radiopaque contrast agent * History of Peripheral Arterial Disease (PAD) with intermittent claudication and/or rest pain * Pregnancy or positive pregnancy test (the participant will be exposed to ionising radiation during the fluoroscopy procedure) * Any other significant disease or disorder which, in the opinion of the recruiting physician, may put the participants at risk because of participation in the study, or may influence the result of the study or the participant's ability to participate

Locations (1)

Royal Berkshire NHS Foundation Trust

Reading, United Kingdom