Assessment of Squamous Cell Carcinoma antigen2 in Verruca Vulgaris
1 other identifier
observational
50
1 country
1
Brief Summary
This study aims to assess the expression of SCCA2 in the skin of patients with warts and to detect its correlation with characteristics of warts.
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 2022
Shorter than P25 for all trials
1 active site
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 Start
First participant enrolled
May 1, 2022
CompletedFirst Submitted
Initial submission to the registry
June 1, 2022
CompletedFirst Posted
Study publicly available on registry
June 8, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2023
CompletedJune 10, 2022
June 1, 2022
6 months
June 1, 2022
June 7, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Assessment of Squamous Cell Carcinoma Antigen2 in Verruca Vulgaris
Immunohistochemical staining: investigators will use monoclonal antibodies to SCCA2 (SERPINB4/ SCCA2 antibody). Immunohistochemical staining will be performed the pattern of immunostaining for SCCA2 will be evaluated in both the epidermis and dermis of wart lesions. The immunohistochemical score (IHC) range will be as follows: 0: negative expression of SCCA2; 1+: weak expression of SCCA2; 2+: moderate expression of SCCA2; and 3+: strong expression of SCCA2.
through study completion, an average of 1 year
Interventions
Immunohistochemical staining
Eligibility Criteria
primary care clinic
You may qualify if:
- Patients present with warts (verruca vulgaris type).
You may not qualify if:
- Subjects who presenting with allergic diseases or other dermatological diseases or had a history of squamous cell carcinoma will be excluded from this study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (1)
Sohag University
Sohag, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Ashraf Ahmed Abd El-Latif Abd El-Latif, Lecturer
Director
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident of Dermatology and Venereology
Study Record Dates
First Submitted
June 1, 2022
First Posted
June 8, 2022
Study Start
May 1, 2022
Primary Completion
November 1, 2022
Study Completion
January 1, 2023
Last Updated
June 10, 2022
Record last verified: 2022-06