- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07472062
Development of a Non-Invasive Prognostic Test for Graves Orbitopathy (GoPro)
March 11, 2026 updated by: University Hospital, Ghent
The aim of this research project is to develop a non-invasive, simple, robust, and sensitive prognostic test that can identify hyperthyroidism patients who are at risk of developing Graves' Orbitopathy.
This phase of the study is a research phase in which we analyze blood samples and tear fluid using standard laboratory equipment and software.
The aim is to identify biomarkers that can detect patients at risk of developing Graves' Orbitopathy.
Offering more personalized advice, treatment, and follow-up could potentially prevent the clinical consequences or limit their severity.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
90
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Ghent, Belgium, 9000
- Ghent University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- healthy control OR diagnosis of hyperthyroidism OR diagnosis of Graves' Orbitopathy
Exclusion Criteria:
- <18 y/o
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Healthy controls
Schirmer's test
|
Collection of tears with Schirmer's test
|
|
Other: Hyperthyroidism
Schirmer's test
|
Collection of tears with Schirmer's test
|
|
Other: Graves' Orbitopathy
Schirmer's test
|
Collection of tears with Schirmer's test
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Biomarkers found in tears collected at Baseline
Time Frame: Baseline
|
During a one-day study visit (Baseline visit), tears will be collected from all study participants via a Schirmer's test.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 13, 2023
Primary Completion (Actual)
June 25, 2024
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
March 5, 2026
First Submitted That Met QC Criteria
March 11, 2026
First Posted (Actual)
March 16, 2026
Study Record Updates
Last Update Posted (Actual)
March 16, 2026
Last Update Submitted That Met QC Criteria
March 11, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Endocrine System Diseases
- Genetic Diseases, Inborn
- Autoimmune Diseases
- Immune System Diseases
- Eye Diseases
- Eye Diseases, Hereditary
- Graves Disease
- Exophthalmos
- Orbital Diseases
- Goiter
- Thyroid Diseases
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Graves Ophthalmopathy
- Hyperthyroidism
Other Study ID Numbers
- BC-09628
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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