Interleukin-6 in Plaque Psoriasis and Its Possible Role in Disease Severity
1 other identifier
observational
50
1 country
1
Brief Summary
This study aimed to evaluate serum IL-6 levels in plaque psoriasis patients and investigate their correlation with disease severity.
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 Nov 2023
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
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
October 31, 2024
CompletedFirst Submitted
Initial submission to the registry
May 24, 2025
CompletedFirst Posted
Study publicly available on registry
June 3, 2025
CompletedJune 3, 2025
May 1, 2025
1 year
May 24, 2025
May 25, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Disease severity
Disease severity was assessed using the Psoriasis Area and Severity Index (PASI), categorizing patients into mild (PASI \<5), moderate (PASI 5-10), and severe (PASI \>10) groups.
3 months post-procedure
Study Arms (2)
Patients group
Patients with plaque psoriasis.
Control group
Sex- and age-matched healthy control individuals.
Interventions
The enzyme-linked immunosorbent assay (ELISA) was utilized in order to determine the levels of IL-6 in the serum
Eligibility Criteria
This cross-sectional work had been performed on 30 individuals with plaque psoriasis and 20 sex- and age-matched healthy controls.
You may qualify if:
- Age above 18 years.
- Both sexes.
- Patients clinically diagnosed with plaque psoriasis.
You may not qualify if:
- Patients who had received any treatment for psoriasis in the last three months.
- Patients with other types of psoriasis.
- Those currently receiving systemic treatment.
- Individuals with other inflammatory diseases.
- Pregnant or lactating women.
- Those using contraceptive pills.
- Patients with metabolic conditions like diabetes mellitus or thyroid disorders.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Tanta Universitylead
Study Sites (1)
Tanta University
Tanta, El-Gharbia, 31527, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt.
Study Record Dates
First Submitted
May 24, 2025
First Posted
June 3, 2025
Study Start
November 1, 2023
Primary Completion
October 31, 2024
Study Completion
October 31, 2024
Last Updated
June 3, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- After the end of study for one year.
- Access Criteria
- The data will be available upon a reasonable request from the corresponding author.
The data will be available upon a reasonable request from the corresponding author after the end of study for one year.