NCT07001904

Brief Summary

This study aimed to evaluate serum IL-6 levels in plaque psoriasis patients and investigate their correlation with disease severity.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

November 1, 2023

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2024

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

May 24, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

June 3, 2025

Completed
Last Updated

June 3, 2025

Status Verified

May 1, 2025

Enrollment Period

1 year

First QC Date

May 24, 2025

Last Update Submit

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.

Other: Enzyme-linked immunosorbent assay (ELISA)

Control group

Sex- and age-matched healthy control individuals.

Other: Enzyme-linked immunosorbent assay (ELISA)

Interventions

The enzyme-linked immunosorbent assay (ELISA) was utilized in order to determine the levels of IL-6 in the serum

Control groupPatients group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Tanta University

Tanta, El-Gharbia, 31527, Egypt

Location

MeSH Terms

Interventions

Enzyme-Linked Immunosorbent Assay

Intervention Hierarchy (Ancestors)

Immunoenzyme TechniquesImmunoassayImmunologic TechniquesInvestigative TechniquesImmunosorbent TechniquesImmunohistochemistryMolecular Probe Techniques

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

The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

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.

Locations