Trichoscopy as a Monitoring Tool for Activity and Remission in Pemphigus Vulgaris: A Clinical Study Supported by Immunological Evaluation.
1 other identifier
observational
62
0 countries
N/A
Brief Summary
Pemphigus vulgaris (PV) is a potential life-threatening autoimmune bullous disorder presenting with multiple erosions and flaccid blisters that can involve both mucous membrane and skin. The microscopic findings include intraepithelial blisters caused by acantholysis of keratinocytes as the consequence of autoantibody formation. The antibodies are mainly IgG autoantibodies mostly directed against desmoglein 1 and 3 (Dsg 1, 3), which are adhesion molecules expressed on the surface of keratinocytes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2025
Shorter than P25 for all trials
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
First Submitted
Initial submission to the registry
March 3, 2025
CompletedFirst Posted
Study publicly available on registry
March 7, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedMarch 7, 2025
February 1, 2025
1 year
March 3, 2025
March 3, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Trichoscopy as a monitooring tool
for activity and remission in PV
1 year
Study Arms (3)
Group 1
cases of PV with disease activity
Group 2
cases of PV with disease remission
Group 3
control group
Interventions
Trichoscopy will be done on patients with PV disease activity and remission
Eligibility Criteria
Patients will be recruited from those attending the Bullous outpatient clinic of department of Dermatology, Assiut University Hospitals with the diagnosis of pemphigus vulgaris. Patients will be included in the study after obtaining a written informed consent. And after the approval of the faculty of medicine ethics committee. An age and sex matched healthy volunteers will be recruited as a control group.
You may qualify if:
- Patients with clinical and histopathological diagnosis of pemphigus vulgaris will be included.
- Pemphigus patients are categorized as active or remittent.
You may not qualify if:
- Other forms of pemphigus.
- Patients who are previously treated with rituximab.
- Patients with any concomitant dermatological diseases.
- Patients with other autoimmune diseases.
- Pregnancy and lactation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (29)
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PMID: 35925475BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principle investigator
Study Record Dates
First Submitted
March 3, 2025
First Posted
March 7, 2025
Study Start
May 1, 2025
Primary Completion
May 1, 2026
Study Completion
May 1, 2026
Last Updated
March 7, 2025
Record last verified: 2025-02