Trials / Completed
CompletedNCT05344482
Evaluation of the Effectiveness of Secukinumab in Patients With Moderate to Severe Plaque Psoriasis
A Retrospective Multicenter Study for the Assessment of Effectiveness of Secukinumab as Assessed by Psoriasis Area and Severity Index With Subcutaneous Administration in Adult Patients With Moderate to Severe Plaque Psoriasis in Turkish Population
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 277 (actual)
- Sponsor
- Novartis Pharmaceuticals · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study was a real-life study which was based on secondary data collection from the electronic or paper medical records from the Dermatology Clinics of the 14 University, Training \& Research Hospitals in Turkey. Data were extracted between 02 September 2020 and 29 April 2021.
Detailed description
The study was a retrospective, multicenter, cohort study which was based on data collection at week 4,16 and 52 of secukinumab treatment of moderate to severe plaque psoriasis. The observational design of the study allowed data collection about secukinumab treatment patterns and clinical and demographic characteristics of plaque psoriasis patients treated with secukinumab for 52 weeks in Turkey. The adults included in the study were treated with secukinumab for 52 weeks. The adults with no available data of PASI scores at specific time points (4, 16 and 52 weeks) and no definite description of treatment cessation were excluded. The study population consisted of adults treated with secukinumab for 52 weeks and adults dropped out before 52 weeks with available data of PASI scores at 4, 16 and 52 weeks and definite description of treatment cessation. Retrospective data collection from secondary sources (hospital medical records) allowed time and cost saving since description of patients' characteristics, analyses of outcomes of interest and their determinants could be made in a short period of time. The study consisted of the following periods: * The index date was the date of initiation of secukinumab * The study (index) period was between 18 May 2018 to 31 May 2020 * The follow-up (post-index) period was 4,16 and 52 weeks post-index
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Secukinumab | Included all the patients treated with secukinumab |
Timeline
- Start date
- 2020-07-09
- Primary completion
- 2021-08-31
- Completion
- 2021-08-31
- First posted
- 2022-04-25
- Last updated
- 2022-07-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05344482. Inclusion in this directory is not an endorsement.