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Clinical trial

Mainstreaming of Clinical Genomic Sequencing for Rare Disease in Ontario, Canada: Protocol for a Province-wide Hybrid Type 2 Implementation-effectiveness Trial

NCT07799792 is registered in ClinicalTrials.gov with The Hospital for Sick Children as lead sponsor.

NCT NCT07799792
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Registry record

As filed in ClinicalTrials.gov.

Title
Mainstreaming of Clinical Genomic Sequencing for Rare Disease in Ontario, Canada: Protocol for a Province-wide Hybrid Type 2 Implementation-effectiveness Trial
Lead sponsor
The Hospital for Sick Children
Phase
Observational
Overall status
Not yet recruiting
Start date
September 1, 2026
Completion date
August 31, 2027
Enrollment
100 (estimated)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

evaluation of mainstreamed models of genetic service delivery, genetic disease, neurodevelomental disorders