Actively Recruiting
Short-term Treatment Satisfaction in Hidradenitis Suppurativa Patients Initiated on Cosentyx in Routine Clinical Practice in Saudi Arabia
Led by Novartis Pharmaceuticals · Updated on 2025-12-30
77
Participants Needed
4
Research Sites
81 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Short-term Treatment Satisfaction in Hidradenitis Suppurativa Patients Initiated on Cosentyx in Routine Clinical Practice in Saudi Arabia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female adults 18 years of age or older at the time of data collection
- Confirmed diagnosis of active moderate to severe Hidradenitis Suppurativa
- Have not previously received secukinumab; first dose within one month of signing informed consent
- May be using antibiotics or have undergone surgery as part of routine care
- Agree to sign informed consent and complete questionnaires
You will not qualify if you...
- Not meeting all inclusion criteria
- Refusal to participate or to sign informed consent
- History of off-label use of biological treatments or JAK inhibitors
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
Novartis Investigative Site
Riyadh, SAU, Saudi Arabia, 11525
Actively Recruiting
2
Novartis Investigative Site
Jeddah, Saudi Arabia, 21391
Actively Recruiting
3
Novartis Investigative Site
Jeddah, Saudi Arabia, 23311
Actively Recruiting
4
Novartis Investigative Site
Riyadh, Saudi Arabia, 11211
Actively Recruiting
Research Team
N
Novartis Pharmaceuticals
CONTACT
N
Novartis Pharmaceuticals
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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