Your session is about to expire
← Back to Search
Embolization Agent
Embolization with Embosphere Microspheres for Knee Osteoarthritis Pain
N/A
Recruiting
Research Sponsored by Shivank Bhatia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
WOMAC score >30
Minimum of prior 12 weeks of failed response to conservative therapy for knee osteoarthritis, which may include one or more of: Oral or topical NSAIDS, opioid medications, intra-articular injection of glucocorticoids or hyaluronic acid, physical therapy.
Must not have
Local infection of the target knee(s)
Active malignancy other than non-melanomatous skin cancer
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 52 weeks (post embolization surgery)
Awards & highlights
No Placebo-Only Group
Summary
This trial will test a permanent embolic for treating knee osteoarthritis by blockage of the geniculate artery.
Who is the study for?
This trial is for adults aged 40-80 with moderate to severe knee osteoarthritis who haven't improved after at least 12 weeks of standard treatments like NSAIDs, steroid injections, or physical therapy. Participants must have synovitis, be able to undergo an MRI, and not have advanced arthritis (Kellgren-Lawrence grade >3), prior knee replacement, certain health conditions that affect embolization procedures, allergies to contrast agents without prophylaxis options, active cancers (except skin cancer), local infections in the knee area or a sensitivity to gelatin.
What is being tested?
The study tests Embosphere Microspheres used in geniculate artery embolization as a treatment for pain from moderate to severe knee osteoarthritis. The goal is to see how effective and safe this permanent blockage procedure is compared to other treatments.
What are the potential side effects?
Potential side effects may include discomfort at the injection site, allergic reactions due to materials used during the procedure such as iodinated contrast agents or gelatin products within the microspheres. There might also be risks associated with catheter-based interventions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My knee or hip pain is severe, based on a score above 30.
Select...
I have tried treatments like painkillers, injections, or physical therapy for my knee arthritis for at least 12 weeks without improvement.
Select...
I have pain in the front area of my knee.
Select...
I am between 40 and 80 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My target knee is infected.
Select...
I have a cancer diagnosis that is not non-melanoma skin cancer.
Select...
I am pregnant, breastfeeding, or planning to become pregnant soon.
Select...
I have had knee replacement surgery.
Select...
I have a condition that prevents me from undergoing procedures involving catheters or embolization.
Select...
I have rheumatoid arthritis.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 52 weeks (post embolization surgery)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 52 weeks (post embolization surgery)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in knee pain as assessed by the WOMAC
Incidence of treatment related adverse events
Secondary study objectives
Change in knee pain
Change in knee pain as assessed by VAS
Incidence of adverse events
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Embosphere Microspheres groupExperimental Treatment1 Intervention
Participants in this group who are receiving standard of care (SOC) embolization surgery for the treatment of moderate to severe knee osteoarthritis will receive the Embospheres Microspheres during scheduled SOC surgery.
Find a Location
Who is running the clinical trial?
Shivank BhatiaLead Sponsor
1 Previous Clinical Trials
4 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My target knee is infected.My knee or hip pain is severe, based on a score above 30.I have tried treatments like painkillers, injections, or physical therapy for my knee arthritis for at least 12 weeks without improvement.Your pain level, measured on a scale from 0 to 100, is higher than 50.I have a cancer diagnosis that is not non-melanoma skin cancer.I am pregnant, breastfeeding, or planning to become pregnant soon.I have pain in the front area of my knee.I have had knee replacement surgery.I have a condition that prevents me from undergoing procedures involving catheters or embolization.You are allergic to iodinated contrast agents and there is no way to prevent or manage the allergic reaction.I am between 40 and 80 years old.The doctor will consider any other health conditions that may prevent you from participating in the study.I have rheumatoid arthritis.You are allergic to gelatin.
Research Study Groups:
This trial has the following groups:- Group 1: Embosphere Microspheres group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger