NCT07730619

Brief 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.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
140

participants targeted

Target at P50-P75 for all trials

Timeline
5mo left

Started Dec 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress90%
Dec 2022Dec 2026

Study Start

First participant enrolled

December 1, 2022

Completed
3.6 years until next milestone

First Submitted

Initial submission to the registry

July 16, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

July 28, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2026

Last Updated

July 28, 2026

Status Verified

July 1, 2026

Enrollment Period

4 years

First QC Date

July 16, 2026

Last Update Submit

July 22, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • General Information

    Age, gender, occupation, education, height, weight, abdominal circumference, history of smoking or excessive drinking, dietary preferences, sleep quality, exercise status

    12/1/2022-12/1/2024

  • Psoriasis related information

    The duration of illness, the name and administration scheme of the biological agent, the age when using the biological agent, the age of the first onset of psoriasis, the body surface involved area (BSA) of the skin lesions when injecting the first dose of biological agent, whether to comply with medical advice, whether to have psoriasis comorbidity, whether to treat other diseases at the same time, whether to have a family history of psoriasis, whether to involve joints, whether to involve special parts, whether to have infectious diseases during the treatment period, whether to vaccinate COVID-19 vaccine

    12/1/2022-12/1/2024

Secondary Outcomes (2)

  • Laboratory testing indicators

    12/1/2022-12/1/2024

  • Imaging examination

    12/1/2022-12/1/2024

Study Arms (2)

Recurrent group

Recurrence after biological therapy

Diagnostic Test: Diagnosis and Physical Examination of Psoriasis

Control group

No recurrence after treatment with biological agents

Diagnostic Test: Diagnosis and Physical Examination of Psoriasis

Interventions

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

Control groupRecurrent group

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

This study retrospectively selected plaque psoriasis patients who received biologic treatment in the dermatology department of our hospital from December 2022 to December 2024.

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

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

Xi'an, Shaanxi, 710061, China

Location

MeSH Terms

Conditions

Recurrence

Interventions

Diagnosis

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

July 16, 2026

First Posted

July 28, 2026

Study Start

December 1, 2022

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 30, 2026

Last Updated

July 28, 2026

Record last verified: 2026-07

Locations