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Clinical Trials/NCT04951479
NCT04951479
Completed
Not Applicable

Geniculate Artery Embolization for Knee Osteoarthritis

Anish Ghodadra1 site in 1 country11 target enrollmentNovember 3, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Anish Ghodadra
Enrollment
11
Locations
1
Primary Endpoint
Change in KOOS Pain Score
Status
Completed
Last Updated
last year

Overview

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.

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.

Registry
clinicaltrials.gov
Start Date
November 3, 2021
End Date
October 26, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Anish Ghodadra
Responsible Party
Sponsor Investigator
Principal Investigator

Anish Ghodadra

Assistant Professor

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • 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')
  • Grade 1, 2, or 3 osteoarthritis on the Kellgren-Lawrence grading scale on knee x-ray in the last 6 months
  • Pain must be refractory to 3 months of medical management (which may include a combination of oral analgesics, intraarticular steroids, viscosupplementation, opioid therapy, etc)
  • Patients willing and able to consent to the study

Exclusion Criteria

  • Kidney dysfunction defined as an estimated GFR \< 60 mL/min
  • Acute knee injury
  • Current local infection
  • Prior ipsilateral knee replacement surgery
  • Infectious or inflammatory arthritis
  • History of contrast allergy resulting in anaphylaxis
  • INR (International Normalization Ratio) \> 1.6
  • Platelets \< 50,000
  • Significant atherosclerosis that would limit angiography
  • Active malignancy

Outcomes

Primary Outcomes

Change in KOOS Pain Score

Time Frame: Baseline and 6 months from treatment

Change in pain score 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 change in KOOS pain score will be the primary outcome measure. Minimum score is 0 and maximum is 100. higher score is better outcome

Secondary Outcomes

  • Change in Knee-related Functionality(Baseline and 6 months from treatment)
  • Change in 30-second Chair Stand Test(Baseline and 6 months from treatment)
  • Change in KOOS Quality of Life Scale(Baseline and 6 months from treatment)
  • 6-minute Walk Test(Baseline and 6 months from treatment)

Study Sites (1)

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