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Recent discoveries with Quebec Pain Registry data

2022 – 2 studies published with data from QPR

2021 – 2 studies published with data from QPR

2020 – 3 studies published with data from QPR

2019 – 2 studies published with data from QPR

2018 – 2 study published with data from QPR

2017 – 3 study published with data from QPR

2016 – 5 studies published with data from QPR

2015 – 3 studies published with data from QPR

2013 – 1 study published with data from QPR

 

The Quebec Pain Registry

The Quebec Pain Registry is an administrative and research database which provides standardized data on a large cohort of chronic pain patients who are described using a set of common demographic and clinical measures based on uniform and validated measurement tools. This unique database, unlike any other in the world, will allow researchers to better understand chronic pain, to improve pain management and treatment.

It was conceived in 2007 as a strategic initiative of the Quebec Pain Research Network.

Number of patients enrolled in the Registry: 9363

The Quebec Pain Registry is the foundation of a province wide clinical infrastructure and is available on a cost recovery model to:

  • Facilitate and stimulate clinical pain research for both academia and industry
  • Provide standardized data on a large cohort of patients with chronic non-cancer pain
  • Provide accelerated access to well-characterized datasets for multisite clinical trials
  • Provide a greater understanding of the impact of chronic pain on society