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Clinical Trials in China / NCT07730619
Active, not recruiting Observational

To Explore the Influencing Factors and Solutions for Patients With Plaque Psoriasis Undergoing Relapse

NCT07730619 · tracked via the Priya Life Science China tracker
Sponsor
First Affiliated Hospital Xi'an Jiaotong University
Phase
Observational
Started
2022-12-01
Last updated
2026-07-28

Condition(s) studied

Plaque PsoriasisBiologic AgentsRelapseInfluence Factors

Investigational drug(s) / intervention(s)

Diagnosis and Physical Examination of Psoriasis

Diagnosis and Physical Examination of Psoriasis: This study divided patients with plaque psoriasis treated with biological agents into a recurrent group and a non recurrent group based on whether they recurred or not

Study summary

In recent years, an increasing number of patients who have experienced poor efficacy or adverse drug reactions using traditional treatment regimens have received biologic therapy and achieved satisfactory treatment results. However, we also found that some patients have poor reactions to biological agents. Biological agents are often the final treatment choice for most patients, and patients often have high expectations for this treatment plan. Therefore, exploring the factors that affect the efficacy of biological agents and effective follow-up treatment plans when there is poor response to biological agents is of great significance for the treatment of psoriasis patients.

The main research objective of this project is to observe and record the clinical characteristics and efficacy of plaque psoriasis patients treated with biological agents in the real world. 2. Explore the influencing factors of recurrence in plaque psoriasis patients receiving biological therapy in the real world, in order to increase awareness and awareness of this phenomenon, and provide guidance for preventing recurrence after biological therapy. 3. Record the follow-up treatment plans or response measures for recurrent patients, and compare the efficacy of different treatment plans.

This study is a case-control study that recruited patients with plaque psoriasis who have received biological therapy for more than half a year. A questionnaire survey was conducted to understand their general information, disease-related clinical data, and laboratory examination data. Univariate analysis was used to compare all variables between groups, and logistic regression analysis was performed on variables with statistical differences. Corresponding ROC curves were then drawn. Perform a separate analysis of the Adalimumab group according to the above steps. In addition, descriptive analysis was conducted on the characteristics that may be related to the disease in the recurrence group, and the efficacy of different treatment plans after recurrence was compared.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * Diagnosed as plaque psoriasis. * Received biological therapy for more than six months. * Voluntarily participate in this study, with normal communication and understanding abilities. * Recurrent group: Patients with initial treatment effective (PGA or BSA improvement reduced by more than 75% from baseline), PGA ≥ 3 or BSA decreased by less than 50% from baseline after a period of time \[218\], and who were treated in the dermatology department of our hospital. * Control group: Treatment effective (PGA maintained at 0/1 or BSA improvement decreased by more than 75% from baseline), and no recurrence as mentioned in ④ occurred. Exclusion Criteria: * Patients with other types of psoriasis. * Pregnant patients * Patients who refuse to cooperate with medical staff questionnaire surveys or refuse to provide auxiliary testing or examination materials.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Dermatology Department of the First Affiliated Hospital of Xi'an Jiaotong University Xi'an Shaanxi

More First Affiliated Hospital Xi'an Jiaotong University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07730619 on ClinicalTrials.gov ↗ ← All trials in China