Phase
Condition
Prostate Cancer
Prostate Disorders
Sexually Transmitted Diseases (Stds)
Treatment
Ibuprofen or Naproxen
PSA test
Ibuprofen 400 mg, TID
Clinical Study ID
Ages 18-80 Male
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male patients age between 18-80 years old with a screening PSA > 3 ng/ml beingconsidered for additional diagnostic testing (e.g., MRI, biopsy)
Normal digital rectal examination within the past two years. A documented normaldigital rectal examination by another physician or advanced practice provider (NP,PA, etc) is acceptable.
No clinical symptoms concerning for acute urinary tract infection (e.g. dysuria,malodorous urine, positive urine culture)
Exclusion
Exclusion Criteria:
History of hypersensitivity or allergy to ibuprofen or NSAIDs.
History of peptic ulcer disease, GI bleeding or NSAIDs induced GI adverse events
Known bleeding disorders
Known severe chronic kidney disease: eGFR < 30 mL/min/1.73 m2
Heart failure, significant heart disease
Poorly controlled hypertension
Active urinary tract infections or bacteriuria
Concomitant use of 5-alpha reductase inhibitors (finasteride, dutasteride) unlesspatient has been taking it for at least 6 months
Known prostate cancer or underwent prostate MRI or biopsy in the last year
Urinary tract instrumentation in the past 6 weeks (catheter, cystoscopy)
Concomitant anti-inflammatory or steroidal drugs
Concomitant dual-antiplatelet or anticoagulant therapy use except aspirin 81 mgalone
Know history of severe liver disease determined by abnormal liver function tests (elevated AST or ALT > 3X ULN based on exiting history or labs)
Any other medical contraindication to NSAIDs
Study Design
Study Description
Connect with a study center
University of Chicago Medical Center
Chicago, Illinois 60637
United StatesActive - Recruiting
Albany Medical Center
Albany, New York 12208
United StatesActive - Recruiting
Penn State-Hershey Medical Center
Hershey, Pennsylvania 17033
United StatesActive - Recruiting
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