Effect of Probenecid on Synovial Fluid ATP Levels in CPPD

Overview

This study will investigate the hypothesis that probenecid, a medication currently used for gout, reduces levels of ATP in the joint fluid of patients with calcium pyrophosphate deposition disease (CPPD), another common type of crystal-related arthritis. There is good evidence that CPPD results from an excess of ATP in joints. The investigators will measure levels of ATP in joint fluid before and after 5 days of treatment with probenecid. This study will serve to rationalize larger studies of probenecid in CPPD.

Full Title of Study: “ANK-dependent ATP Efflux Causes Calcium Pyrophosphate Deposition in Cartilage”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: September 30, 2021

Detailed Description

Objective: The objective of this study is to determine whether pharmacologic doses of the drug probenecid significantly decrease ATP and inorganic pyrophosphate (PPi) levels in the synovial fluid of patients with calcium pyrophosphate deposition disease (CPPD). The investigators have considerable evidence that synovial fluid ATP levels are high in patients with this disease and these high levels lead to calcium pyrophosphate (CPP) crystal formation which then produces acute and chronic arthritis. The investigators have identified the transmembrane protein known as ANK as the chief regulator of ATP levels in and around cartilage. Probenecid blocks function of ANK in vitro. The purpose of this study is to determine if probenecid used at normal doses are sufficient to block ANK function in vivo and whether this results in reduced ATP and PPi levels in synovial fluid. Research design: This is a randomized un-controlled trial of probenecid vs. no drug in patients with a joint effusion and known CPPD. Methodology: Power analysis based on an 80% chance to show a 20% difference in ATP levels in the treatment group resulted in a sample size of 20 patients in each group. Patients with known CPPD and a joint effusion will have an arthrocentesis to remove 2 ml of synovial fluid from their joint. Fluid will be sent to the investigators' research laboratory and ATP and PPi levels will be measured. Patients will be randomized to treatment with 2 grams/day of probenecid or no therapy. After 5 days, the remainder of the joint fluid will be removed and tested for ATP and PPi levels. The investigators will compare differences in ATP and PPi levels in the probenecid treated and the untreated group.

Interventions

  • Drug: Probenecid
    • Treatment

Arms, Groups and Cohorts

  • Experimental: Probenecid
    • These patients will receive 5 days of probenecid.
  • No Intervention: No intervention
    • These patients will receive no intervention.

Clinical Trial Outcome Measures

Primary Measures

  • ATP levels in synovial fluid
    • Time Frame: 5 days
    • The investigators will measure levels of ATP in synovial fluid from patients with CPPD before and after treatment with probenecid compared to patients receiving no therapy. ATP levels are measured with a standard bioluminescent assay.

Participating in This Clinical Trial

Inclusion Criteria

Inclusion criteria:

  • Age >21 years, – CPPD diagnosed by Ryan /McCarty criteria – Joint effusion in a shoulder or knee Exclusion Criteria:

Exclusion criteria:

  • Inability to sign informed consent – Age <21 years – History of renal stones – Significant renal dysfunction (CKD >stage 2) – Blood dyscrasias – Current use of drugs which interact with probenecid – Concurrent gout – Active infection, including bacteremia and overlying cellulitis – Recent joint trauma – Intra-articular corticosteroids in the affected joint within three months

Gender Eligibility: All

Minimum Age: 21 Years

Maximum Age: 99 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • VA Office of Research and Development
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Ann K Rosenthal, MD, Principal Investigator, Clement J. Zablocki VA Medical Center, Milwaukee, WI
  • Overall Contact(s)
    • Ann K Rosenthal, MD, (414) 384-2000, Ann.Rosenthal@va.gov

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