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Biological
Platelet Rich Plasma Injection for Knee Osteoarthritis
Phase < 1
Waitlist Available
Led By Christian Wuescher, MD
Research Sponsored by University of Toledo Health Science Campus
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
Study Summary
This trial will be testing whether platelet-rich plasma injections can help ease pain for people with knee osteoarthritis.
Eligible Conditions
- Osteoarthritis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Correlation of outcomes with whole blood and platelet rich plasma (PRP) concentrations
Functional status outcome using the Timed up and go (TUG) test, 1 year
Functional status outcome using the Timed up and go (TUG) test, 3 months
+9 moreSecondary outcome measures
Correlation of outcomes and patient demographics and co-morbidities
Emergency room utilization, 1 year
Emergency room utilization, 3 months
+6 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Participants receiving a platelet rich plasma injectionExperimental Treatment1 Intervention
All patients in the study will be receiving a platelet rich plasma injection, and we will be following their clinical outcomes
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Platelet Rich Plasma Injection
2016
N/A
~20
Find a Location
Who is running the clinical trial?
University of Toledo Health Science CampusLead Sponsor
40 Previous Clinical Trials
16,520 Total Patients Enrolled
1 Trials studying Osteoarthritis
60 Patients Enrolled for Osteoarthritis
Christian Wuescher, MDPrincipal InvestigatorUniversity of Toledo
Ashley Schneider, MDStudy DirectorUniversity of Toledo
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a diagnosed rheumatologic disease that affects your knee.You have had surgery on your knee in the past.Your knee pain is not caused by nerve issues, pain referred from other areas, or an infection in the knee joint.You have a serious heart condition.Your immune system is weakened or suppressed.You are currently taking medication to prevent blood clots or to stop platelets from sticking together.You have a history of a serious mental illness with hallucinations or delusions.You have had knee pain or swelling for more than 3 months.You have knee pain that is rated as at least a 3 out of 10 on a pain scale.You are currently using drugs through intravenous (IV) injection.You recently had a serious knee injury that caused pain and swelling.You have received a knee injection in the past 3 months.
Research Study Groups:
This trial has the following groups:- Group 1: Participants receiving a platelet rich plasma injection
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Who else is applying?
What state do they live in?
Washington
Other
Pennsylvania
Ohio
How old are they?
18 - 65
65+
What site did they apply to?
University of Toledo, Health Science Campus
What portion of applicants met pre-screening criteria?
Did not meet criteria
Met criteria
How responsive is this trial?
Most responsive sites:
- University of Toledo, Health Science Campus: < 24 hours
Typically responds via
Email
Average response time
- < 1 Day
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