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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT05013970
Other study ID # S62757
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date August 1, 2021
Est. completion date December 2022

Study information

Verified date December 2023
Source Universitaire Ziekenhuizen KU Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Disabling symptoms of osteoarthritis are seen in approximatively 10% of people over 55 years old. Many patients suffer from persistent pain symptoms from moderate osteoarthritis despite optimal medical treatment. For these patients, several minimally-invasive surgical treatments have been proposed, including arthroscopic lavage and debridement; however, none of these treatments have been proven effective compared to sham treatment. Recently, catheter-directed embolotherapy of the geniculate arteries has been propagated as a real alternative to medical management in patients with mild to moderate knee osteoarthritis unresponsive to conservative medical management.


Description:

Disabling symptoms of osteoarthritis are seen in approximatively 10% of people over 55 years old. Traditionally, treatment of symptomatic knee osteoarthritis is based on administration of pain relievers, including nonsteroidal anti-inflammatory drugs, in case of mild to moderate symptoms; major joint replacement surgery (total joint arthroplasty) is performed in cases of severe and end-stage osteoarthritis. However, many patients suffer from persistent pain symptoms from moderate osteoarthritis despite optimal medical treatment. For these patients, several minimally-invasive surgical treatments have been proposed, including arthroscopic lavage and debridement; however, none of these treatments have been proven effective compared to sham treatment. Recently, catheter-directed embolotherapy of the geniculate arteries has been propagated as a real alternative to medical management in patients with mild to moderate knee osteoarthritis unresponsive to conservative medical management. Transcatheter embolotherapy was performed using imipenem/cilastin sodium or 75 micron calibrated Embozene microspheres and follow-up was performed by physical examination, questionnaires (VAS-score and WOMAC-scores) and MR-imaging (WORMS-score). Results of these trials confirmed that catheter-directed embolotherapy is a safe procedure without any major adverse events. WOMAC pain scores dropped dramatically from 12.2 +/- 1.9 before the procedure to 3.3 +/- 2.1 at 1 month after the procedure and to 1.7 +/- 2.2 at 4 months after the procedure. Additionally, MR imaging at 2 years of follow-up could not demonstrate any osteonecrosis or progression of degenerative changes.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: - Presence of knee pain - Kellgren-Lawrence (KL) grade 1-3 assessed by weight-bearing knee radiographs - Local tenderness around the knee - Clinical failure after 3 months or more of conservative therapies, including oral nonsteroidal anti-inflammatory drugs and/or oral opioid agents and physical therapy, stretching, muscle strengthening and/or intra-articular injection of hyaluronic acid - Persistent moderate to severe knee pain (VAS > 50 mm) for more than 3 months - Patient is able to give consent Exclusion Criteria: - Previous knee surgery - Local infection - BMI > 40 kg/m2 - Advanced atherosclerosis - Rheumatoid arthritis, malignancy, renal insufficiency, other conditions contra-indicating femoropopliteal angiography - Usage of anticoagulants such as eliquis or coumarine (Asaflow allowed) - Allergy to iodinated contrast medium or any other allergy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Clinical assessment
Clinical assessment including Visual Analog Scale (VAS) for Knee Pain, and Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire
Radiographic imaging
MRI of the knee

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen KU Leuven

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analog Scale (VAS) for Knee Pain To measure pain in patients with knee osteoarthritis Within 30 days after catheter-directed embolization
Primary Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire To evaluate symptoms and limitations in patients with knee osteoarthritis Within 30 days after catheter-directed embolization
Primary MRI imaging To depict potential asymptomatic, but radiologically visible side-effects At day 30 after catheter-directed embolization
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