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Active, not recruitingNCT07472062GoProUpdated Mar 16, 2026

Development of a Non-Invasive Prognostic Test for Graves Orbitopathy

An interventional study of Schirmer's test in Graves Orbitopathy and Hyperthyroidism, sponsored by University Hospital, Ghent. Active, not recruiting at 1 site in Belgium. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-16.

Sponsored by University Hospital, Ghent · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 2 years 9 months after the study started (first participant enrolled May 2023, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

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Conditions studied

  • Graves Orbitopathy
  • Hyperthyroidism
03

In context

Graves Ophthalmopathy

199 studies on the registry are indexed under Graves Ophthalmopathy; 58 are open to participants now.

This study's enrollment of 90 is above the median of 63 across 146 interventional studies indexed under Graves Ophthalmopathy.

Browse Graves Ophthalmopathy studies →

Lead sponsor

University Hospital, Ghent is the lead sponsor of 689 studies on the registry; 160 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 4 (80%) 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

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

  • healthy control OR diagnosis of hyperthyroidism OR diagnosis of Graves' Orbitopathy

Exclusion criteria

Exclusion Criteria:

  • \<18 y/o
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
90 participants (actual)

Study arms

  • Other
    Healthy controls

    Schirmer's test

    Other: Schirmer's test

  • Other
    Hyperthyroidism

    Schirmer's test

    Other: Schirmer's test

  • Other
    Graves' Orbitopathy

    Schirmer's test

    Other: Schirmer's test

Interventions

  • OtherSchirmer's test

    Collection of tears with Schirmer's test

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What researchers measure

Primary outcomes

  1. Biomarkers found in tears collected at Baseline

    During a one-day study visit (Baseline visit), tears will be collected from all study participants via a Schirmer's test.

    Time frame: Baseline

07

Study locations

1 site
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from May 2023 to primary completion in Jun 2024, 13 months.

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

Registered
Mar 5, 2026
First posted
Mar 16, 2026
StartActual
May 13, 2023
Primary completionActual
Jun 25, 2024
CompletionEst.
Dec 31, 2026
Last update
Mar 16, 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.
No changes since tracking began. The registry record was last updated on Mar 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07472062
Responsible party
Sponsor
First posted
Mar 16, 2026
Start date
May 13, 2023
Primary completion
Jun 25, 2024
Completion
Dec 31, 2026 (estimated)
Last update
Mar 16, 2026

Oversight

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

Not currently enrolling

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

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Discussion

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