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Graves' OrbitopathyMISS:GONCT07870161

Microbiota and Immune SignatureS of Graves' Disease and Orbitopathy

A study testing Aspiration 0 in people with Graves' Orbitopathy and Graves' Disease, run by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico at 1 site in Italy.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Graves' disease (GD) is the commonest cause of hyperthyroidism, characterised by anti-thyrotropin receptor autoantibodies (TRAb) persistently stimulating the thyroid gland. Around 30-50% GD patients also develop Graves' orbitopathy (GO), an orbital inflammation causing disfigurement and visual problems… Read more about this study

Who is it for?
Ages 18 to 75 yearsHealthy volunteers can take part
What is being tested?
Aspiration 0
Could I receive a placebo?
No, everyone receives an active treatment
How many people
67 participants
Where
1 siteItaly
Study dates
25 Feb 2025to 31 Oct 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age: 18-75 years old
  • Sex: Male and Female
  • Signed informed consent
  • Patients will present one of the following conditions:
  • Basedow/Graves' Disease (GD), defined as hyperthyroidism with positive TRAb at diagnosis and without Graves's Ophthalmology (GO).
  • Graves' Ophthalmology (GO), defined as patients with GD and also GO, characterised by inflammatory signs (periorbital and/or eyelid edema, eyelid hyperemia, edema or hyperemia of the plica/caruncle, conjunctival hyperemia, orbital/ocular pain at rest, ocular/orbital pain on eye movement, chemosis) and/or exophthalmos or proptosis (≥23 mm) and/or limitation of eye movements with/without diplopia, and/or optic nerve involvement and/or decrease in visual acuity.
  • Nodular goiter (NG), difined as an increase in dimension of the thyroid gland and one or more thyroid nodules, with negative TRAb, anti-thyroglobulin antibodies (TgAb) and anti-thyroperoxidase (TPOAb).

Who cannot join

  • Pregnancy or six months post partum and/or breast feeding
  • Presence of severe cronic disease and/or granulomatous (ex: sarcoidosis)
  • Prior splenectomy
  • Prior organ or bone marrow or hematopoietic stem cells transplant

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico

    Milan, 20122

Other trials in Italy

About this study

Official title: Studio Del Microbiota e Del Profilo Immunologico Nella Malattia di Basedow/Graves e Nell'Oftalmopatia Basedowiana (Microbiota and Immune SignatureS of Graves' Disease and Orbitopathy)

Graves' disease (GD) is the commonest cause of hyperthyroidism, characterised by anti-thyrotropin receptor autoantibodies (TRAb) persistently stimulating the thyroid gland. Around 30-50% GD patients also develop Graves' orbitopathy (GO), an orbital inflammation causing disfigurement and visual problems; moderate-to-severe forms represent 5% of GO cases and are associated with high risk of sight loss. Some risk factors for GO have been identified (i.e. smoking, stress, high TRAb titres, severe hyperthyroidism) and predictive models for disease development and response to treatment have been attempted, but are still missing/incomplete. The GD/GO pathogenesis is multifactorial and not fully understood, including a complex interplay between genetic predisposition and environmental factors. A loss of immune tolerance has been observed; in particular an imbalance between T Helper 17 (Th17) and T Regulatory (Treg). The gut microbiota modulates the differentiation of immature T cells in the gut-associated-lymphoid-tissue and microbiota alterations seem involved in autoimmune diseases, including GD/GO. Indeed, a dysbiosis of the gut microbiota may alter the Treg/T17 balance and thus impact on immune homeostasis.

The international EU-FP7 funded study "Investigation of Novel biomarkers and Definition of the role of the microbiome In Graves' Orbitopathy" (INDIGO) represented one of the first investigations about the role of gut microbiota in GD and GO diseases (https://cordis.europa.eu/project/id/612116), spanning across eight centres of four European countries: United Kingdom (Cardiff, Merthyr Tydfil, Newcastle upon Tyne and Moorfields), Italy (Milan and Pisa), Belgium (Brussels) and Germany (Essen). The INDIGO consortium provided the human gut microbiome analysis by 16S rRNA sequencing, performed on faecal samples of 105 patients (59 GD, 46 GO) and 41 controls enrolled between October 2014 and June 2016. It was discovered an increase of Actinobacteria phylum in both GD and GO compared with controls, and a selective enrichment of Roseburia spp. in moderate-severe GO compared with both GD and controls.

Read more

The first objective of this MISS.GO study is to validate with advanced metagenomics techniques (Shotgun sequencing) the INDIGO study's gut microbiome findings, whose samples were stored in a biobank of UO1 (UNIMI). The Shotgun sequencing allows a deeper taxonomic investigation down to species level, while 16s rRNA sequencing is limited to genus level. Furthermore it increases the chances to detect low abundant species, not possible with 16S rRNA sequencing, and extends the microbiome analysis to yeasts, fungi and a variety of other microorganisms in addition to Bacteria and Archea, to which 16s rRNA sequencing is restricted. Furthermore, this study integrates the metabolomics analysis performed on stored plasma of INDIGO's patients.

The MISS.GO study also includes a prospective phase were 59 subjects (33 GO, 9 GD and 17 controls) were recruited in the Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico of Milan, Italy, to deliver an in depth analysis of the relationship between microbiota and immune system, since:

  1. Advanced Shotgun sequencing is also applied to nasal swabs, in addition to faecal samples. The role of nasal microbiota, and its relationship with gut microbiota, will be explored for the first time in GD and GO patients;
  2. Metagenomics data are integrated with metabolomics and proteomics analysis performed on plasma, faecal and nasal samples;
  3. Such advanced microbiota's analyses are also integrated with paired immunophenotyping of lymphocytes resident within the organs targeted by autoimmunity in GD and GO patients (thyroid and lymph node) accessed by fine-needle aspiration (FNA), to study the bidirectional modulation between microbiota and immune system.

The final goal of MISS.GO study, thanks to such integrated analysis of fecal and nasal metagenomics, metabolomics and metaproteomics, together with paired tissue-resident immunophenotyping, is to improve the current knowledge of GD and GO pathogenesis, aiming to identify prognostic GD and GO markers, predictive factors for GO development, and key microbiota and immune signatures that can be exploited for prevention, mitigation and therapeutic strategies.

Being tested
Aspiration 0
Keywords
Graves' Disease, Basedow, Graves' Orbitopathy, Microbiota, Immune Signatures, Microbiota and Immune signature of Graves' disease and Orbitopathy
Medical subject headings
Graves Ophthalmopathy, Graves Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Aspiration 0Other

    Also called Fine needle aspiration of thyroid and neck

    Ultrasound guided fine needle aspiration of thyroid and neck

Study groups in NCT07870161
Study groupRoleWhat they receive
Participants with Graves' Disease, without Graves' OphthalmologyOtherNot described
Receives: Other: Aspiration 0
Participants with Graves' Disease and Graves OphthalmologyOtherNot described
Receives: Other: Aspiration 0
Patients with nodular goiterOtherControl arm
Receives: Other: Aspiration 0

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Treg and Th17 linfocites

    Measured: Patients are sampled at enrollment (Day 0)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Oct 2026
  2. Study start25 Feb 2025
  3. Primary completion14 Sep 2026
  4. Study completion31 Oct 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
67 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07870161
Sponsor's protocol ID
ID 4995
Acronym
MISS:GO
Status last verified
Oct 2026
First submitted
6 Oct 2026
Last updated
13 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Aspiration 0 in people with Graves' Orbitopathy and Graves' Disease, run by Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 13 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Treg and Th17 linfocites (time frame: Patients are sampled at enrollment (Day 0)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Oct 2026.

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