Actively Recruiting

Phase 2
Age: 18Years - 80Years
All Genders
NCT04939623

Novel Use of Probenecid to Alleviate Symptoms of Opioid Withdrawal

Led by University of Calgary · Updated on 2026-05-01

40

Participants Needed

1

Research Sites

165 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The proposed clinical trial will address the problem of opioid withdrawal. Opioids are essential for pain-relief in the short term, but their continued use is associated with a host of adverse effects. People living with chronic pain who were initiated on opioid therapy now find themselves with a major life-changing problem - dependence on opioid medications. Opioid withdrawal symptoms are a key barrier to decreasing or stopping their opioid medication. Currently, there are few medications that ameliorate the symptoms of opioid withdrawal. This problem is a major part of the opioid crisis in Canada, and impacts people across all demographics and socioeconomic status. A misconception is that only individuals with opioid use disorder are susceptible to opioid withdrawal; on the contrary, appropriate use of prescription opioids to manage pain can lead to significant symptoms of opioid withdrawal when it is reduced or stopped. Patients in Alberta who are at risk for opioid withdrawal, either from prescribed use or misuse will be primarily impacted by this trial. The investigators have recently explored the underlying causes of opioid withdrawal and identified an important target in the spinal cord that is responsible for producing withdrawal symptoms in rats and mice. The target, a protein called pannexin-1 (Panx1), is located throughout the body, specifically in the brain and spinal cord. Using sophisticated biochemical, genetic, and pharmacological techniques, the investigators demonstrated how Panx1 on immune cells is implicated in the production of opioid withdrawal symptoms after cessation of fentanyl and morphine in opioid dependent rodents. The investigators then attenuated these symptoms of withdrawal using probenecid, a drug which inherently blocks Panx1 activity. Because probenecid is a safe and clinically available drug, the findings could be immediately translated into clinical therapy to support people who are struggling with the symptoms of opioid withdrawal and provide clinicians with a safe and effective option for caring for this population.

CONDITIONS

Official Title

Novel Use of Probenecid to Alleviate Symptoms of Opioid Withdrawal

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults with chronic pain aged 18 years or older on the day of enrollment
  • Currently taking daily opioid pain medication and planning to taper the dose
  • Must complete at least one voluntary opioid dose reduction during the 12-week study
  • Glomerular filtration rate (GFR) greater than 50 mL/min
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Allergy to probenecid or related drugs
  • History of uric acid kidney stones or any type of kidney stones if unknown
  • Known deficiency of G6PD enzyme
  • Active gout in any joint
  • Current use of certain drugs that interact with probenecid, including specific penicillins, carbapenems, benzodiazepines, ketorolac, oseltamivir, methotrexate, or mycophenolate
  • Current use of drugs that may hide withdrawal symptoms like clonidine or tizanidine
  • Current use of drugs that may reduce probenecid's effect, such as high dose salicylates over 325 mg daily
  • Pregnancy or breastfeeding
  • Any major medical condition that could affect safety or follow-up
  • Participation in another clinical trial within 30 days prior to enrollment

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Richmond Road Diagnostic and Treatment Centre

Calgary, Alberta, Canada, T2T 5C7

Actively Recruiting

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Research Team

T

Tammy Eberle

CONTACT

L

Lori Montgomery

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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