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Real-World Study on the Burden of Hidradenitis Suppurativa

P

PeriPharm

Status

Not yet enrolling

Conditions

Hidradenitis Suppurativa (HS)

Treatments

Other: No Intervention: Observational Cohort

Study type

Observational

Funder types

Other

Identifiers

NCT07323303
PROxy85HS

Details and patient eligibility

About

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.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patient diagnosed with HS;
  2. Aged ≥18 years;
  3. Able to read and understand French or English;
  4. Willing and able to provide written informed consent.

Exclusion criteria

1. Participation in an interventional study for HS.

Trial design

100 participants in 1 patient group

Patient with HS
Description:
Patient diagnosed with HS
Treatment:
Other: No Intervention: Observational Cohort

Trial contacts and locations

0

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Central trial contact

Jean Lachaine, PhD

Data sourced from clinicaltrials.gov

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