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Despite the significant impact of HS on patients' quality of life (QoL) and daily functioning, there remains limited real-world evidence describing the burden of this condition in Canada. HS is an under-recognized and often misdiagnosed condition, with a substantial psychological and physical burden on patients. Understanding the real-world experiences of individuals living with HS in Canada can help identify unmet needs and inform patient-centered care approaches.
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1. Participation in an interventional study for HS.
100 participants in 1 patient group
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Jean Lachaine, PhD
Data sourced from clinicaltrials.gov
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