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Clinical Trials/NCT05629494
NCT05629494
Recruiting
Phase 4

Effect of Non-steroidal Anti-inflammatory Drugs on Serum Prostate Specific Antigen Level

Albany Medical College3 sites in 1 country198 target enrollmentSeptember 27, 2022

Overview

Phase
Phase 4
Intervention
PSA test
Conditions
Prostate Cancer
Sponsor
Albany Medical College
Enrollment
198
Locations
3
Primary Endpoint
Difference in the extent of changes in PSA level between the study groups
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Prostate cancer is the most frequently diagnosed cancer in men in the Unites States. Nearly 1 million prostate biopsy procedures are performed in the United States annually and elevated prostate-specific antigen (PSA) level is the primary reason for prostate biopsy in > 90% of cases. However, at the PSA levels which trigger prostate biopsy, often no cancer is found in prostate biopsy specimens. PSA test can be elevated due to reasons other than cancer such as inflammation or natural variation in the level. Investigators plan to treat men with elevated PSA level with over the counter anti-inflammatory medications (ibuprofen, naproxen) to see if the PSA level will decrease to an acceptable level.

Detailed Description

It's known that PSA level can be elevated due to reasons other than prostate cancer including benign prostatic hypertrophy, prostatitis or other urinary tract infections, non-infectious inflammation, and physiologic variation over time. Consequently, nearly 50% of prostate biopsy procedures performed due to elevated PSA level do not yield any cancer , but still expose the patients to the risks of the procedure related complications (discomfort/pain, anxiety, bleeding, infection, and cost). Thus, measures to improve the reliability of PSA test, and potentially avoiding unnecessary procedures, are of significant importance to the patient and healthcare system. It is common practice to check PSA level annually. PSA test results can vary over time, either due to the imprecision in the analysis and/or due to the biologic variability. This can result in an apparent rise in PSA level when no clinically meaningful rise had occurred. Its estimated that the average lab variation in PSA was approximately 6% and the average biologic variation about 14%. This, it is recommended that isolated elevation in PSA level should be confirmed after several weeks, and before proceeding with further interventions, including prostate biopsy. Sub-clinical, histologic Inflammation (presence of inflammatory cells) within the prostate tissue and its effect on PSA level has been reported in various settings. In two population-based studies, men who were regularly using over the counter (OTC) nonsteroidal anti-inflammatory drugs (NSAIDs, e.g ibuprofen, naproxen) had lower PSA levels compared to non-users. Currently, two strategies are utilized in clinical practice to ensure that the PSA level is truly elevated: 1. Repeat PSA test after several weeks or 2. A short course of OTC NSAIDs, and then repeat PSA test Investigators propose to conduct a randomized study to determine the effect of NSAIDs on PSA level compared to the biologic variations in PSA level noted upon repeat testing.

Registry
clinicaltrials.gov
Start Date
September 27, 2022
End Date
December 1, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Badar M. Mian

Professor of Urology

Albany Medical College

Eligibility Criteria

Inclusion Criteria

  • Male patients age between 18-80 years old with a screening PSA \> 3 ng/ml being considered for additional diagnostic testing (e.g., MRI, biopsy)
  • Normal digital rectal examination within the past two years. A documented normal digital 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 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) unless patient 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)

Arms & Interventions

Repeat serum PSA test

Repeat PSA test at 6 (± 1) weeks, without any treatment

Intervention: PSA test

Treatment with NSAIDS

Treatment with Ibuprofen 400 mg, 3 times per day, then repeat PSA test at 6 (± 1) weeks

Intervention: Ibuprofen 400 mg, TID

Treatment with NSAIDS

Treatment with Ibuprofen 400 mg, 3 times per day, then repeat PSA test at 6 (± 1) weeks

Intervention: PSA test

Outcomes

Primary Outcomes

Difference in the extent of changes in PSA level between the study groups

Time Frame: 6 weeks

Difference in PSA levels, within and between groups

Participants with change in PSA level to below the age-specific PSA threshold

Time Frame: 6 weeks

To determine if changes in PSA level were sufficient to avoid intervention

Secondary Outcomes

  • Determine the incidence of acute kidney injury following a short course of ibuprofen(1 year)
  • Durability of the change in PSA levels(1 to 1.5 year)
  • Changes in voiding symptoms as measured by the International Prostate Symptom Score(3-12 months)

Study Sites (3)

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