GAE: Geniculate Artery Embolization for Knee Osteoarthritis
Study Details
Study Description
Brief Summary
The purpose of this study is to perform a prospective case series to determine efficacy of transcatheter arterial embolization in treating knee osteoarthritis related pain, improving functionality, and reducing opiate usage in patients with mild to moderate knee osteoarthritis who have failed conservative management.
The Gel-Bead embolization particles will be used to perform geniculate artery embolization (GAE) for the purposes of treatment of osteoarthritis-related knee pain.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
Management of mild and moderate knee osteoarthritis is curated to each specific patient and their needs, their quality of life, and desired goals. Weight loss is advised for overweight and obese patients. All patients should attempt extended-duration exercise/physical therapy and realignment therapy. If these conservative lifestyle modifications fail to reduce pain, topical and oral non-steroidal anti-inflammatories are indicated. Escalation of care from here is controversial. Some clinicians opt for adjunctive treatments such as intra-articular injection of steroids or viscosupplementation. Unfortunately, pain alleviation from intra-articular steroids is short-lasting and a recent meta-analysis demonstrated no significant difference between intra-articular hyaluronic acid injection and placebo injection. Finally, weak opioids are an option for patients who continue to have pain despite all the aforementioned treatment measures. Joint replacement is reserved for patients with severe osteoarthritis.
Patients who fail conservative, medical management pose a challenge to clinicians. For decades, there have been no interventions available to these patients between the controversial intra-articular hyaluronic acid injection and joint replacement. Interventional radiology (IR) may provide one possible solution. Geniculate artery embolization (GAE) is a minimally-invasive procedure that has historically been performed for patients with recurrent hemarthrosis. It was recently applied to patients with moderate osteoarthritis refractory to maximal medical management. Several studies have been performed and have found that GAE is safe and improves pain.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Gel-Bead Embolization
|
Device: Gel-Bead embolization
OptiSphere is FDA approved for the embolization of hypervascular tumors. The product is crosslinked with glutaraldehyde, which improves the mechanical strength of the spheres and provides controlled degradation after implant. The spherical shape provides smooth embolic delivery and even, predictable distribution. In this study the Optispheres will be used for Geniculate artery embolization (GAE) which is a minimally-invasive procedure that has historically been performed for treatment of patients with recurrent knee hemarthrosis. Embolization is a procedure in which material is used to block small blood vessels. Angiogenesis, or growth of new vessels, has been implicated in the initiation and maintenance of joint inflammation. GAE has been applied to patients with moderate osteoarthritis-related pain refractory to maximal medical management with preliminary studies demonstrating a reduction in patient pain.
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Outcome Measures
Primary Outcome Measures
- Overall efficacy of treatment [Baseline and 6 months from treatment]
Average change in pain of at least 10 points based on the KOOS Pain questionnaire. The KOOS Pain score runs from 0 (no pain) to 100 (worst pain). The percentage of patients with at least 10 point increase in KOOS pain score will be the primary outcome measure.
Secondary Outcome Measures
- Change in knee-related functionality [Baseline and 6 months from treatment]
Average change in the KOOS Function in Sport and Recreation (FSR). The KOOS FSR score runs from 0 (no symptoms) to 100 (worst symptoms).
- Change in KOOS Quality of Life Scale [Baseline and 6 months from treatment]
Average change in in the KOOS Quality of Life Scale (QoL) score. The KOOS QoL score runs from 0 (no symptoms) to 100 (worst symptoms). An increase in this value is considered improvement.
- 6-minute walk test [Baseline and 6 months from treatment]
Average change in in 6-minute walk test in meters.
- 30-second chair stand test [Baseline and 6 months from treatment]
Average change in 30-second chair stand test in number of chair stands. An increase in this value is considered improvement.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Patients between ages 18 and 75 with moderate/severe knee pain secondary to primary osteoarthritis. Moderate/severe pain will be defined as pain 30 mm to 100 mm on the Visual Analog Pain Scale (where 0 denotes 'no pain' and 100 mm denotes worst pain imaginable')
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Grade 1, 2, or 3 osteoarthritis on the Kellgren-Lawrence grading scale on knee x-ray in the last 6 months
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Pain must be refractory to 3 months of medical management (which may include a combination of oral analgesics, intraarticular steroids, viscosupplementation, opioid therapy, etc)
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Patients willing and able to consent to the study
Exclusion Criteria:
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Kidney dysfunction defined as an estimated GFR < 60 mL/min
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Acute knee injury
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Current local infection
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Prior ipsilateral knee replacement surgery
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Infectious or inflammatory arthritis
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History of contrast allergy resulting in anaphylaxis
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INR (International Normalization Ratio) > 1.6
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Platelets < 50,000
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Significant atherosclerosis that would limit angiography
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Active malignancy
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Active pregnancy
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Appropriate candidate for knee replacement surgery determined by clinical and physical examination
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Recent within 3 months, or active cigarette user
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | UPMC Shadyside | Pittsburgh | Pennsylvania | United States | 15232 |
Sponsors and Collaborators
- Anish Ghodadra
Investigators
- Principal Investigator: Anish Ghodadra, MD, University of Pittsburgh
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- STUDY19010266