Actively Recruiting
Platelet Rich Plasma Versus Corticosteroids in Hip Osteoarthritis Pain
Led by LifeBridge Health · Updated on 2025-03-14
54
Participants Needed
1
Research Sites
92 weeks
Total Duration
On this page
Sponsors
L
LifeBridge Health
Lead Sponsor
H
Hip Society
Collaborating Sponsor
AI-Summary
What this Trial Is About
Prospective, single-center that may go on to being multicenter, randomized trial comparing platelet rich plasma (PRP) versus corticosteroid injection for the treatment of symptoms of Hip osteoarthritis. The purpose of the study is to determine which therapy provides a greater reduction in patient reported outcome measures of pain and function.
CONDITIONS
Official Title
Platelet Rich Plasma Versus Corticosteroids in Hip Osteoarthritis Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form provided
- Willingness to comply with all study procedures and available for the study duration
- Male or female aged 21 to 80 years
- Radiographic diagnosis of Kellgren-Lawrence grade II or III hip osteoarthritis
- Indicated for a hip injection to treat hip osteoarthritis symptoms
You will not qualify if you...
- Any injection into the target hip within the past three months
- Current skin infection over the injection area
- Current or previous diagnosis of chronic pain
- Opioid tolerance at screening (daily usage for a week or longer of specified opioid doses)
- Allergy to any ingredients or medications used in the study
- Treatment with another investigational drug or intervention for pain
- Diagnosis of diabetes mellitus
- Female participants who are pregnant or planning pregnancy within three months or study duration
- Any physical or psychological condition that would prevent participation according to the investigator's opinion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sinai Hospital of Baltimore
Baltimore, Maryland, United States, 21215
Actively Recruiting
Research Team
M
Martin Gesheff, DHSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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