Your session is about to expire
← Back to Search
Control for Cuff Tear Arthropathy
N/A
Waitlist Available
Led By C. Benjamin Ma, MD
Research Sponsored by University of California, San Francisco
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 preop, 1 year post/op, 2 years post/op
Awards & highlights
Study Summary
This trial will test if ibuprofen reduces post-operative pain and opiate use after shoulder surgery.
Eligible Conditions
- Cuff Tear Arthropathy
- Rotator Cuff Tears
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ preop, 1 year post/op, 2 years post/op
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~preop, 1 year post/op, 2 years post/op
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Ibuprofen
Secondary outcome measures
Assessment of functional shoulder outcome score: ASES
Assessment of functional shoulder outcome score: DASH
Assessment of functional shoulder outcome score: SF-12
+2 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: ControlActive Control1 Intervention
Ibuprofen 400mg by mouth three times daily. Patients will also receive the standard opiate medication (hydrocodone/acetaminophen 10mg/325mg) for the UCSF orthopaedic clinic for postoperative pain control.
Group II: PlaceboPlacebo Group1 Intervention
Placebo tablet by mouth three times daily. Patients will also received the standard opiate medication (hydrocodone/acetaminophen 10mg/325mg) for the UCSF orthopaedic clinic for postoperative pain control.
Find a Location
Who is running the clinical trial?
University of California, San FranciscoLead Sponsor
2,506 Previous Clinical Trials
15,238,455 Total Patients Enrolled
C. Benjamin Ma, MDPrincipal InvestigatorUniversity of California, San Francisco
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
Share this study with friends
Copy Link
Messenger