Your session is about to expire
← Back to Search
Nonsteroidal Anti-inflammatory Drug
Naproxen for Heterotopic Ossification
Phase < 1
Waitlist Available
Led By Stephen Aoki, M.D.
Research Sponsored by University of Utah
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 75 days after surgery
Awards & highlights
Study Summary
In a brief summary the study would like to evaluate the effectiveness of Naproxen in preventing radiographically detected heterotopic ossification following hip arthroscopy for the treatment of femoroacetabular impingement.
Eligible Conditions
- Heterotopic Ossification
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 75 days after surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~75 days after surgery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of participants with documented Heterotopic Ossification (HO) in the Naproxen group vs Placebo group
Secondary outcome measures
Naproxen
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: NaproxenActive Control1 Intervention
• Group 1: Naproxen 500 mg twice daily for three weeks following surgery beginning postoperative day #1
Group II: PlaceboPlacebo Group1 Intervention
• Group 2: Placebo twice daily for three weeks following surgery beginning postoperative day #1
Find a Location
Who is running the clinical trial?
University of UtahLead Sponsor
1,099 Previous Clinical Trials
1,778,581 Total Patients Enrolled
Stephen Aoki, M.D.Principal InvestigatorUniversity of Utah Orthopedics Center
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger