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NCT03460054: CGNR

The Canadian Glomerulonephritis Registry and Translational Research Initiative

Status unknown Last updated 9 March 2018
What this trial tests

trial in Glomerular Nephritis in 300 participants. Status unknown.

Timeline
19 October 2017
Primary endpoint
30 December 2022
30 June 2023

Quick facts

Lead sponsorUniversity Health Network, Toronto
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment300
Start date19 October 2017
Primary completion30 December 2022
Estimated completion30 June 2023
Sites1 location across Canada

Conditions studied

Sponsor

University Health Network, Toronto

Who can join

Adults 18 to 80, any sex, with Glomerular Nephritis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Glomerulonephritis (GN) is one of the most important causes of kidney failure in Canada. These comprise a group of "rare" diseases (\<5 per 250,000 population), yet GN is a leading cause of kidney failure and accounts annually for close to 20% of incident cases of end stage kidney disease (ESKD) in Canada. Prevention of progression to kidney failure is possible, however several barriers and gaps in knowledge challenge our ability to provide patients with individualized effective therapy. These include a lack of sensitive non-invasive tools for monitoring disease activity, prognosis, and response to therapy. A gap in understanding of the core molecular processes underlying the development and progression of GN, and a lack of cohesive networks for evaluation of novel treatment approaches contribute to a lack of targeted and personalized therapies for GN. To address these challenges we will create a national, multi-dimensional platform for application of human-based molecular research and advanced therapeutics in GN.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The Canadian Glomerulonephritis Registry (CGNR) and Translational Research Initiative: Rationale and Clinical Research Protocol.
    Hildebrand AM, Barua M, Barbour SJ, Tennankore KK, et al · · 2022 · cited 5× · PMID 35450151 · DOI 10.1177/20543581221089094

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