Clin2
NCT07799792Possibly a fitNot yet recruiting

Genome-wide sequencing for rare diseases in Ontario

Evaluation of Mainstreamed Models of Genetic Service DeliveryGenetic DiseaseNeurodevelomental Disorders

Part of Genetic & congenital clinical trials.

This study looks at how genome-wide sequencing (a test that reads all your DNA) is being used for people with rare diseases in Ontario. It aims to improve how this test is offered and followed up, which may help you get clearer answers about your condition.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
Any age
Study type
Observational

Who can take part

  • You have had genome-wide sequencing in Ontario.
  • You are a clinician (not a geneticist) in Ontario who has ordered this test for a patient.
  • You are a caregiver of a patient who had this test through a non-geneticist clinician in Ontario.
  • If you are a caregiver, you must be 18 years old or older.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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