Ankylosing Spondylitis

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16-80
SponsorSohag University

About this trial

The goal of this observational study is to measure the serum level of cytokines IL-17, IL-38,IL-41, and gene expression of HLA-B27 gene in ankylosing spondylitis patients and healthy control group.

The main question it aims to answer is:

Does the disease activity, severity, serum level of cytokines (IL-17, IL-38, and IL-41) are affected by the HLA-b27 gene positivity?

Researchers will compare the serum level of cytokines IL-17, IL-38,IL-41, and gene expression of HLA-B27 gene in ankylosing spondylitis patients and healthy control group to see if there significant differences in serum levels of interleukins 17, 38, 41 in AS patients and healthy control group.

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Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

patients who are diagnosed clinically as ankylosing spondylitis (both active or stable), of either sex , who met the Assessment of Spondyloarthritis International Society (ASAS) criteria for axial spondyloarthritis.

Disqualifiers

Patients with any autoimmune disorder, chronic illnesses as diabetes mellitus, acute and chronic infectious diseases, malignancy.

Trial population

Participants will be recruited from the outpatient clinics of Rheumatology and Rehabilitation Department, Sohag University Hospitals.

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

84 Participants
are grouped into 2 trial groups
Group A: Cases
Group B: Healthy Controls

Trial outcomes

Primary outcomes

1

collection of blood samples from paticipants

Time frame
from March 2026 to August 2026
2

measurement of serum level of Interleukin 17 in participants

Time frame
From September 2026 to October 2026
3

Measurement of serum level of Interleukin 38 in participants

Time frame
from September 2026 to October 2026
4

measurement of serum level of Interleukin 41 in participants

Time frame
from September 2026 to October 2026

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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