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Not yet recruitingNCT07907913Updated Oct 30, 2026

SLAMF1 Gene Expression in Ankylosing Spondylitis

An observational study in Ankylosing Spondylitis, sponsored by Assiut University. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by Assiut University · Observational

Updated Oct 30, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

This cross-sectional study aims to evaluate SLAMF1 gene expression levels in patients with ankylosing spondylitis compared with healthy controls.

Read the detailed description

Ankylosing spondylitis is a chronic immune-mediated inflammatory disease affecting the axial skeleton. SLAMF1 is a cell-surface immunoregulatory receptor expressed on immune cells that may play a role in inflammatory responses.

This observational study will measure relative SLAMF1 gene expression by real-time PCR in adult patients with ankylosing spondylitis and age- and sex-matched healthy controls.

02

Conditions studied

  • Ankylosing Spondylitis

Keywords

  • SLAMF1
  • Gene expression
  • Ankylosing spondylitis
  • BASDAI
  • Assiut
03

In context

Spondylitis, Ankylosing

531 studies on the registry are indexed under Spondylitis, Ankylosing; 98 are open to participants now.

This study's planned enrollment of 100 is below the median of 202 across 214 observational studies indexed under Spondylitis, Ankylosing.

Browse Spondylitis, Ankylosing studies →

Lead sponsor

Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adult patients aged 18 years or older diagnosed with ankylosing spondylitis and age- and sex-matched healthy controls at Assiut University Hospitals.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult Egyptian patients aged 18 years or older
  • Diagnosed with ankylosing spondylitis according to established clinical criteria (patient group)
  • Apparently healthy adults matched for age and sex (control group)
  • Written

Exclusion criteria

Exclusion Criteria:

  • Other concomitant systemic or inflammatory rheumatic diseases
  • Active acute infection at blood sampling
  • Current or active anticancer treatment
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients with Ankylosing Spondylitis

    Adult patients diagnosed with ankylosing spondylitis.

  • Healthy Controls

    Age- and sex-matched apparently healthy adults without inflammatory rheumatic disease.

06

What researchers measure

Primary outcomes

  1. SLAMF1 gene expression

    Mean relative SLAMF1 gene expression level measured by real-time quantitative polymerase chain reaction.

    Time frame: Baseline

Secondary outcomes

  1. BASDAI score

    Mean Bath Ankylosing Spondylitis Disease Activity Index score (range 0 to 10, higher scores indicate higher disease activity).

    Time frame: Baseline

  2. Erythrocyte sedimentation rate

    Mean erythrocyte sedimentation rate in millimeters per hour.

    Time frame: Baseline

  3. C-reactive protein

    Mean C-reactive protein level in milligrams per liter.

    Time frame: Baseline

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2026; primary completion for Oct 2027, 12 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 26, 2026
First posted
Oct 30, 2026
StartEst.
Oct 30, 2026
Primary completionEst.
Oct 30, 2027
CompletionEst.
Mar 25, 2028
Last update
Oct 30, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 30, 2026
Show all 1 update
  1. Oct 30, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07907913
Lead sponsor
Assiut University
Responsible party
Mennat-Allah Khaled Tolba Abdelraheem (Assistant Lecturer, Department of Clinical Pathology, Assiut University) — Principal investigator
First posted
Oct 30, 2026
Start date
Oct 30, 2026 (estimated)
Primary completion
Oct 30, 2027 (estimated)
Completion
Mar 25, 2028 (estimated)
Last update
Oct 30, 2026

Study contacts

Mennat Allah K Tolba, Ass Lec
Contact
mennatolba@aun.edu.eg
01093579968
sohair K sayed
study chair · Clinical pathology Department, Assiut University Hospitals

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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