- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07634016
Global Healthcare Study on Psoriasis (GHSP)
June 2, 2026 updated by: Julia Tatjana Maul
The Global Healthcare Study on Psoriasis (GHSP) is an international, multicenter observational study hosted by the University of Zurich (UZH) investigating healthcare access, treatment patterns, disease severity, and quality of life in patients with psoriasis.
The study collects standardized clinical data from routine medical records to identify disparities in healthcare delivery and outcomes across different healthcare systems.
Study Overview
Status
Recruiting
Conditions
Detailed Description
The study employs a combined retrospective and prospective design, collecting data from routine clinical care and medical records spanning from January 2020 through the study conclusion.
Study Type
Observational
Enrollment (Estimated)
9600
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Julia-Tatjana Maul
- Phone Number: +41 76 441 51 09
- Email: julia-tatjana.maul@uzh.ch
Study Contact Backup
- Name: Johannes A Didaskalu, Prof. Dr. med.
- Phone Number: +41 76 36 19 475
- Email: johannes.didaskalu@uzh.ch
Study Locations
-
-
-
Zurich, Switzerland
- Recruiting
- University of Zurich
-
Contact:
- Julia-Tatjana Maul
- Phone Number: +41 76 441 51 09
- Email: julia-tatjana.maul@uzh.ch
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patient populations across world regions seen for psoriasis.
Description
Inclusion Criteria:
- Signed General Consent Form, or equivalent document
- Confirmed diagnosis of Psoriasis
Exclusion Criteria:
- Inability to provide informed consent.
- Datasets with ambiguous or unclear diagnosis.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Global Healthcare Study on Psoriasis
Patients with Psoriasis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psoriasis Area Severity Index (PASI)
Time Frame: Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Composite clinician-assessed measure of psoriasis severity based on erythema, scaling, thickness, and affected body surface area; total score ranges from 0 to 72, with higher scores indicating more severe disease.
|
Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dermatology Life Quality Index (DLQI)
Time Frame: Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Patient-reported measure of dermatology-specific quality of life; total score ranges from 0 to 30, with higher scores indicating greater impairment.
|
Baseline and follow-up visits every 6-12 months for up to 5 years.
|
|
Nail Psoriasis Severity Index (NAPSI)
Time Frame: Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Clinician-assessed measure of nail psoriasis severity based on nail matrix and nail bed involvement; scores range from 0-80 for fingernails and 0-80 for toenails; total score ranges from 0-160, with higher scores indicating more severe nail disease.
|
Baseline and follow-up visits every 6-12 months for up to 5 years.
|
|
Numerical Rating Scale (NRS) for disease severity
Time Frame: Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Patient-reported assessment of psoriasis severity on a numerical rating scale from 0 (no disease) to 10 (most severe disease imaginable).
|
Baseline and follow-up visits every 6-12 months for up to 5 years.
|
|
Physician Global Assessment (PGA)
Time Frame: Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Clinician-assessed global measure of psoriasis severity on a scale from 0 (clear) to 4 (severe).
|
Baseline and follow-up visits every 6-12 months for up to 5 years.
|
|
Body Surface Area (BSA)
Time Frame: Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Percentage of total body surface area affected by psoriasis, ranging from 0% to 100%.
|
Baseline and follow-up visits every 6-12 months for up to 5 years.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Julia-Tatjana Maul, Prof. Dr. med., University of Zurich
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Maul JT, Maul LV, Didaskalu JA, Valenzuela F, Romiti R, Peterson H, Korouri E, Novoa F, Oon HH, Zheng M, Wu JJ, Thyssen JP, Egeberg A, Armstrong AW, Nielsen ML. Correlation between Dermatology Life Quality Index and Psoriasis Area and Severity Index in Patients with Psoriasis: A Cross-sectional Global Healthcare Study on Psoriasis. Acta Derm Venereol. 2024 Mar 12;104:adv20329. doi: 10.2340/actadv.v104.20329.
- Valenzuela F, De La Cruz C, Lecaros C, Fernandez J, Hevia G, Maul LV, Thyssen JP, Vera-Kellet C, Egeberg A, Armijo D, Pizarro C, Riveros T, Correa H, Guglielmetti A, Didaskalu JA, Wu JJ, Griffiths CEM, Romiti R, Maul JT. Comorbidities in Chilean patients with psoriasis: a Global Healthcare Study on Psoriasis. Clin Exp Dermatol. 2022 Dec;47(12):2234-2241. doi: 10.1111/ced.15384. Epub 2022 Oct 28.
- Maul JT, Frohlich F, Maul LV, Stunnenberg R, Valenzuela F, De La Cruz C, Vera-Kellet C, Armijo D, Cesar WG, Carvalho A, Didaskalu JA, Graf N, Egeberg A, Wu JJ, Thyssen JP, Romiti R, Griffiths CEM. Access to psoriasis treatment in Brazil and Chile: A cross-sectional multicentre Global Healthcare Study on Psoriasis. Br J Dermatol. 2023 Mar 30;188(4):533-541. doi: 10.1093/bjd/ljac128.
- Korouri E, Jeong C, Peterson H, Valenzuela F, Romiti R, Didaskalu JA, Egeberg A, Oon HH, Maul LV, Kingston P, Lee K, Huang MY, Yee D, Artiga K, Aguero R, Maul JT, Armstrong AW. Global Comparison of COVID-19 Vaccination Rates among Psoriasis Patients. Life (Basel). 2024 Oct 13;14(10):1297. doi: 10.3390/life14101297.
- Goh E, Nielsen ML, Maul LV, Didaskalu JA, Chularojanamontri L, Guevara BEK, Ji M, Zheng M, Maul JT, Oon HH. Clinical Characteristics and Treatment Patterns of Psoriasis in Asia and Switzerland: Results of the Multicentre Global Healthcare Study on Psoriasis (GHSP). Int J Dermatol. 2026 Jun;65(6):1195-1202. doi: 10.1111/ijd.70183. Epub 2025 Nov 30.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2025
Primary Completion (Estimated)
December 31, 2029
Study Completion (Estimated)
December 31, 2029
Study Registration Dates
First Submitted
June 2, 2026
First Submitted That Met QC Criteria
June 2, 2026
First Posted (Actual)
June 8, 2026
Study Record Updates
Last Update Posted (Actual)
June 8, 2026
Last Update Submitted That Met QC Criteria
June 2, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-00002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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