Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07480720

Systemic Inflammation, Thyroid Autoimmunity and Neuroretinal Changes in Graves Disease

Led by Elazıg Fethi Sekin Sehir Hastanesi · Updated on 2026-03-18

100

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This retrospective observational study aims to evaluate the relationship between systemic inflammatory parameters, thyroid autoimmunity markers, and neuroretinal structures in patients with Graves disease. Medical records of patients diagnosed with Graves disease and healthy control subjects evaluated at Elazığ Fethi Sekin City Hospital between August 2018 and January 2026 will be reviewed. Optical coherence tomography (OCT) measurements, including macular thickness and peripapillary retinal nerve fiber layer (RNFL) thickness, will be analyzed. Laboratory parameters such as complete blood count-derived inflammatory indices, C-reactive protein, thyroid function tests, and thyroid autoantibodies will also be recorded. The study will compare neuroretinal parameters between healthy controls, Graves disease patients without ophthalmopathy, and Graves disease patients with ophthalmopathy, and will investigate potential associations between systemic inflammation, thyroid autoimmunity, and neuroretinal structural changes.

CONDITIONS

Official Title

Systemic Inflammation, Thyroid Autoimmunity and Neuroretinal Changes in Graves Disease

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 6 18 years
  • Diagnosis of Graves' disease (for the patient group)
  • No known thyroid disease in healthy control participants
  • Availability of optical coherence tomography (OCT) measurements and laboratory data
  • Time interval between OCT examination and blood sampling 4 10 days
Not Eligible

You will not qualify if you...

  • Presence of glaucoma, optic neuropathy, or retinal vascular diseases
  • Macular diseases, uveitis, or severe refractive error (high myopia >6 diopters)
  • Diabetic retinopathy
  • History of previous intraocular surgery
  • History of active infection, malignancy, or systemic inflammatory disease
  • Poor-quality OCT measurements (segmentation errors or low signal strength)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Fethi Sekin City Hospital

Elâzığ, Elaziğ, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

SİNEM KESER, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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