Actively Recruiting
Painful Post-Operative Hip Study
Led by University of Wisconsin, Madison · Updated on 2026-02-17
15
Participants Needed
1
Research Sites
40 weeks
Total Duration
On this page
Sponsors
U
University of Wisconsin, Madison
Lead Sponsor
A
Arthroscopy Association of North America
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if the hips of people who undergo revision hip arthroscopy look different from the hips of people whose hip pain is resolved with the first hip arthroscopy and of people who choose the steroid injection for pain management. Participants will complete one PET/MRI scan.
CONDITIONS
Official Title
Painful Post-Operative Hip Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-45 years
- History of unilateral hip arthroscopy
- No fracture, infection, or malignancy 6 months after hip arthroscopy
- No depression or major mental health conditions before the first hip arthroscopy
- No persistent pain requiring opioid use and no history of opioid abuse
- No systemic disease limiting function (ASA physical status classification 3 or less)
- Not currently pregnant
- Persistent pain of 4 or higher on pain scale for at least 6 months after hip arthroscopy
- Undergoing revision hip arthroscopy with no surgery on the other hip
You will not qualify if you...
- No history of unilateral hip arthroscopy
- Fracture, infection, or malignancy present 6 months after hip arthroscopy
- Depression or major mental health conditions before the first hip arthroscopy
- Persistent pain requiring opioid use or history of opioid abuse
- Systemic disease limiting function (ASA physical status classification more than 3)
- Currently pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Wisconsin - Madison
Madison, Wisconsin, United States, 53705
Actively Recruiting
Research Team
A
Amie Armstrong
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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