Short-term Treatment Satisfaction in Hidradenitis Suppurativa Patients Initiated on Cosentyx in Routine Clinical Practice in Saudi Arabia
Survey Assessing Prospective Patient's Short-term Treatment Satisfaction and Quality of Life in Patients With Hidradenitis Suppurativa Initiated on Cosentyx (Secukinumab) in Routine Clinical Practice in Saudi Arabia: ILLUMINATE-SA
Novartis Pharmaceuticals
77 participants
Mar 10, 2025
OBSERVATIONAL
Conditions
Summary
This study aims to assess the treatment satisfaction of HS patients newly started on secukinumab in Saudi Arabia, in terms of patient reported convenience, perceived safety, perceived effectiveness and global treatment satisfaction as measured by the treatment satisfaction questionnaire for medication (TSQM) at week 24 among moderate to severe HS patients.
Eligibility
Inclusion Criteria7
- Male or Female adult patients ≥18 years of age at the time of data collection.
- Patient with a confirmed diagnosis of active moderate to severe HS.
- Secukinumab naive patients (first dose to coincide within one month of the signature of the informed consent) as per locally approved label.
- Patients can be using antibiotics or have undergone surgery as per routine clinical practice.
- Patients agree to sign an informed consent form (ICF) to be able to complete the questionnaires.
- Patient's refusal to be included in the study or refusal to sign the ICF.
- A history of off-label indication uses of biological treatment or JAK inhibitor.
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Interventions
This is an observational study. There is no treatment allocation. The decision to initiate secukinumab will be based solely on clinical judgement.
Locations(4)
View Full Details on ClinicalTrials.gov
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NCT06785779