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Personal Precise Treatment on Psoriasis and Psoriatic Arthritis

Personal Precise Treatment on Psoriasis and Psoriatic Arthritis and Investigate the Mechanisms of Biological Agents Induced Systemic Lupus Erythematosus

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04915105
Enrollment
90
Registered
2021-06-07
Start date
2021-05-31
Completion date
2025-05-31
Last updated
2021-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dermatologic Disease

Keywords

PSO, PSA, SLE, PBMC

Brief summary

Part of psoriasis and psoriatic arthritis patients treated with biologics and met primary failure. Therefore, we are going to create a cell based platform to evaluate the treatment effects of different biologics on psoriasis and psoriatic arthritis patients before prescribed by physicians

Detailed description

PBMCs isolated from psoriasis and psoriatic arthritis and incubated with Group A streptococcus and different biologics for 24 hours. Cytokines expression in the culture supernatants will be measured and the data can be reference for physician's prescription.

Interventions

DIAGNOSTIC_TESTMarkers data from PBMCs

Prescreen markers from patient individual PBMCs treating with streptococcus and different biologics.

Sponsors

Taichung Veterans General Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* 1\. Healthy control without underline disease such as psoriasis and psoriatic arthritis. 2. Psoriasis been diagnosed for over six months and PASI \>10. 3.Psoriatic arthritis been diagnosed for over six months and \>1 swallow and tender joints

Exclusion criteria

* nil

Design outcomes

Primary

MeasureTime frameDescription
PASI score2 weeks to 3 monthsPsoriasis skin condition and severity
swelling joint count and tenderness joint count2 weeks to 3 monthsPSA severity

Secondary

MeasureTime frameDescription
CRP3-6 monthsblood test
DLQI6 monthspaper to investigate patient life quality

Contacts

Primary ContactChung-Yang Yen, MDPhD
vernayen@yahoo.com.tw886423592525

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026