ClinicalTrials.gg
RecruitingNCT06736015MYOSELUpdated Aug 26, 2026

Myo-inositol and Selenium in Indeterminate Thyroid Nodules (TIR3a)

An interventional study of Myo-Inositol 600 mg + Selenium 83 mcg in Thyroid Nodule, sponsored by Regina Elena Cancer Institute. Recruiting at 1 site in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-26.

Sponsored by Regina Elena Cancer Institute · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started Oct 2024; still recruiting 2 years later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Thyroid nodules present a variable risk of malignancy depending on the cytological result obtained from the ultrasound-assisted thyroid fine needle aspiration biopsy. According to the Italian Cytology classification SIAPEC-IAP 2014, the TIR3A nodules are indeterminate nodules with a risk of malignancy lower than 10%. Clinical and instrumental follow-up is recommended in these cases, including repetition of the fine needle aspiration.

A study have demonstrate the effect of a six-month treatment with a supplement containing myo-inositol and selenium on the size and elasticity of benign thyroid nodules.

Our hypothesis is that the use of this supplement can determine a reduction in the size and consistency of the nodule assessed through ultrasound and elastosonography also in cytologically indeterminate (TIR3A) nodules and that treatment can reduce the cellular proliferation of these nodules assessed by immunocytochemistry.

Therefore, we design a prospective randomized pilot study to assess efficacy and safety of myo-inositol and selenium in TIR3a thyroid nosules, comparing treated and untreated patients.

Read the detailed description

Cytological classification of thyroid nodules (TIR 1-5) provides a useful tool in clinical practice. Each TIR class is statistically associated with a certain risk for malignancy, defining the recommended clinical action to undertake. The undetermined diagnosis (TIR 3) should represent less than 20% of patients, with an approximate risk of malignancy of 5-30%. Because of the variable risk of malignancy in the entire TIR 3 category, this is further divided into two groups: TIR 3A (low-risk follicular lesion): a heterogeneous group, with a low expected risk of malignancy (below 10%) and TIR 3B (follicular proliferation or suspected follicular neoplasia) with a higher expected risk of malignancy (15-30%). TIR3A nodules required close clinical and ultrasound follow-up and repetition of fine needle aspiration biopsy is recommended.

Selenium (Se) has the highest concentration in thyroid gland and selenium proteins are involved in thyroid hormone synthesis. Myo-inositol (MI) acts as second messengers both in thyroid differentiation and hormone synthesis and in inhibiting thyroid cells growth by inhibiting PI3K/AKT/mTOR pathway. Inositol is able to reduce NF-KB, a mediator of PI3K/AKT pathway, involved in cellular proliferation. In addition, in vitro studies demonstrated that inositol can reduce apoptosis and angiogenesis, but also inhibit the process of tumor metastasis and invasion by acting on the cytoskeleton. For this reason, this association could have a role in blocking thyroid nodule growth. Evidence from the literature highlights an important role of MI and Se in thyroid physiology and the maintenance of a euthyroid status. Particularly these micronutrients seem fundamental to counteract the onset and the worsening of thyroid alteration that could evolve into different pathological conditions if untreated. In this scenario, MI supplementation seemed to be involved also in the management of thyroidal benign nodules, with a possible effect on the size reduction. Interestingly, the administration of MI plus Se for 6 months of treatment period, was able to induce a morphological change by reducing the size and the stiffness of the nodules classified as class I or II (according to AACE/ACE/AME guidelines) in patients affected by subclinical hypothyroid.

Previous studies demonstrated a beneficial effect on subclinical hypothyroidism, restoring a euthyroid state and reducing both thyroid antibodies and TSH levels, mainly in patients affected by Hashimoto's thyroiditis. Based on these studies, nowadays, in clinical practice, oral supplementation with myoinositol and selenium is widespread and indicated in patients affected by subclinical hypotiroidism with values of TSH in the range 5-10 mcu/I with or without positivity to antibodies TPO-Ab/TG-Ab or in patients affected by Hashimoto's thyroiditis with TSH at the upper limit of the reference range.

The proposed study aims to evaluate the effect of selenium and myoinositol on possible risk factors for malignancy, as proliferation index, elastosonography characteristics (elasticity score) and TSH levels comparing a group of patients with selenium and myoinositol supplementation with a group without supplementation.

02

Conditions studied

  • Thyroid Nodule

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Keywords

  • TIR3A
  • indeterminate thyroid nodules
  • myo-inositol
  • selenium
03

In context

Thyroid Nodule

207 studies on the registry are indexed under Thyroid Nodule; 64 are open to participants now.

This study's planned enrollment of 30 is below the median of 75 across 121 interventional studies indexed under Thyroid Nodule.

Browse Thyroid Nodule studies →

Lead sponsor

Regina Elena Cancer Institute is the lead sponsor of 94 studies on the registry; 51 are open to participants now.

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
No

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 (>18 years old),
  • both sexes,
  • patients presenting thyroid nodules classified as TIR 3A, based on cytological evaluation on sample from the first fine needle aspiration (FNA),
  • written ,
  • Patients with appropriate material for subsequent immunocytochemical analysis of Ki-67 and PCNA

Exclusion criteria

Exclusion Criteria:

  • Patients with diagnosed thyroid of cytological diagnosis other than TIR3A
  • pathological levels of the thyroid stimulating hormone (TSH) which required L-Thyroxine treatment starting
  • pregnancy and/or breastfeeding
Terms in these criteria, in plain language(2)

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.

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

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Myo-inositol and selenium supplementation

    Supplement with Myo-Inositol 600 mg + Selenium 83 mcg once a day for 6 months

    Dietary Supplement: Myo-Inositol 600 mg + Selenium 83 mcg

  • No intervention
    Control

    No intervention

Interventions

  • Dietary supplementMyo-Inositol 600 mg + Selenium 83 mcg

    Drug page: Inositol

    Myo-Inositol 600 mg + Selenium 83 mcg: 1 tablet once a day for 6 months

    Also known as: Tiroxil 4.0

06

What researchers measure

Primary outcomes

  1. Evaluation of differences in elastosonography after six months in patients treated with selenium and myo-inositol and patients not treated (controls)

    Changes in elastosonographic score after treatment (comparing treated and untreated patients)- Score varies from 1 (soft) to 4 (hard)

    Time frame: 6 months

Secondary outcomes

  1. Evaluation of the inibition of the growth of thyroid nodules with Myo-inositol and Selenium supplementation

    Changes in immunocytochemistry proliferation index (such as Ki-67 labeling index, from 0% to 100%) (comparing treated and untreated patients)

    Time frame: 6 months

  2. Evaluation of the differences in thyroid nodules volume in patients treated with selenium and myo-inositol

    Changes in thyroid nodules volume (ml) in patients treated with selenium and myo-inositol (comparing treated and untreated patients)

    Time frame: 6 months

  3. Evaluation of the differences in thyroid hormones in patients treated with selenium and myo-inositol

    Changes in thyroid hormones levels (TSH, FT3, FT4) in patients treated with selenium and myo-inositol (comparing treated and untreated patients)

    Time frame: 6 months

  4. Evaluation of the differences in anti-thyroid antibodies, in patients treated with selenium and myo-inositol

    Changes in anti-thyroid antibodies (AbTg, AbTPO) in patients treated with selenium and myo-inositol (comparing treated and untreated patients)

    Time frame: 6 months

  5. Evaluation of the differences in thyroglobulin in patients treated with selenium and myo-inositol

    Changes in thyroglobulin serum levels in patients treated with selenium and myo-inositol (comparing treated and untreated patients)

    Time frame: 6 months

  6. Correlation of cytological findings to histological parameters (subgroup of patients who will undergo surgical intervention)

    Correlation of cytological findings to histological parameters

    Time frame: 6 months

07

Study locations

1 of 1 sites recruiting
  • Regina Elena National Cancer Institute
    Rome, 00144, Italy
    Recruiting
    • Marialuisa Appetecchia, MD · Contactmarialuisa.appetecchia@ifo.it · 0039 0652666026
    • Marta Bianchini, MD · Sub investigator
    • Marilda Mormando, MD, PhD · Sub investigator
    • Rosa Lauretta, MD · Sub investigator
    • Giulia Puliani, MD, PhD · Sub investigator
    • Ferdinando Marandino, MD · Sub investigator
08

References and documents

Individual participant data

Plan to share: Yes — At the end of the study, anonymized patient data will be shared on garrbox.it repository

Supporting information: Clinical study report

Time frame: After study result publication

Access criteria: GARRbox user and working group

Data sharing details ↗ · gbox.garr.it

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2024 (actual). Primary completion is estimated for Mar 2027, 28 months after the start.

Of 67 non-industry interventional studies with no phase under Thyroid Nodule, half reached primary completion within 30 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 46. This study's planned 28 months is close to that.

Counting every sponsor, half of 71 studies reached it within 30 months; a quarter within 14 and three quarters within 46.

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

Registered
Dec 5, 2024
First posted
Dec 16, 2024
StartActual
Oct 23, 2024
Primary completionEst.
Mar 18, 2027
CompletionEst.
Sep 30, 2027
Last update
Aug 26, 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 Aug 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06736015
Lead sponsor
Regina Elena Cancer Institute
Responsible party
Marialuisa Appetecchia (Chief of the Oncological Endocrinology Unit, Regina Elena Cancer Institute) — Principal investigator
First posted
Dec 16, 2024
Start date
Oct 23, 2024
Primary completion
Mar 18, 2027 (estimated)
Completion
Sep 30, 2027 (estimated)
Last update
Aug 26, 2026

Study contacts

Marialuisa Appetecchia, MD
Contact
marialuisa.appetecchia@ifo.it
0039 0652666026
Giulia Puliani, MD, PhD
Contact
giulia.puliani@ifo.it
0039 065266034
Marialuisa Appetecchia, MD
principal investigator · Regina Elena National Cancer Institute - IRCCS IFO

Oversight

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

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Studies of the drug tested here: Inositol

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