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Thyroid NoduleMYOSELNCT06736015

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

A study testing Myo-Inositol 600 mg + Selenium 83 mcg in people with Thyroid Nodule, run by Regina Elena Cancer Institute at 1 site in Italy.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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%. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Thyroid Nodule
What is being tested?
Myo-Inositol 600 mg + Selenium 83 mcg
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteItaly
Study dates
23 Oct 2024to 30 Sep 2027
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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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 Informed consent,
  • Patients with appropriate material for subsequent immunocytochemical analysis of Ki-67 and PCNA

Who cannot join

  • Patients with diagnosed thyroid malignancies of cytological diagnosis other than TIR3A
  • pathological levels of the thyroid stimulating hormone (TSH) which required L-Thyroxine treatment starting
  • pregnancy and/or breastfeeding

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Marialuisa Appetecchia, MD contact

0039 0652666026

marialuisa.appetecchia@ifo.it

Giulia Puliani, MD, PhD contact

0039 065266034

giulia.puliani@ifo.it

Italy1 site, 1 recruiting
  • Regina Elena National Cancer Institute

    Rome, 00144

    Marialuisa Appetecchia, MD, 0039 0652666026, marialuisa.appetecchia@ifo.it

    Marta Bianchini, MD

    Recruiting

Other trials in Italy

About this study

Official title: Use of Myo-inositol and Selenium in Patients With Indeterminate Thyroid Nodules (TIR3A)

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.

Read more

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.

Conditions
Thyroid Nodule
Being tested
Myo-Inositol 600 mg + Selenium 83 mcg
Keywords
TIR3A, indeterminate thyroid nodules, myo-inositol, selenium
Medical subject headings
Thyroid Nodule

What participants receive

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

  • Myo-Inositol 600 mg + Selenium 83 mcgDietary supplement

    Also called Tiroxil 4.0

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

Study groups in NCT06736015
Study groupRoleWhat they receive
Myo-inositol and selenium supplementationExperimentalSupplement with Myo-Inositol 600 mg + Selenium 83 mcg once a day for 6 months
Receives: Dietary Supplement: Myo-Inositol 600 mg + Selenium 83 mcg
ControlNo interventionNo intervention

What is being measured

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

  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)

    Measured: 6 months

Secondary outcomes (6)
  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)

    Measured: 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)

    Measured: 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)

    Measured: 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)

    Measured: 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)

    Measured: 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

    Measured: 6 months

Timeline

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

  1. First posted16 Dec 2024
  2. Study start23 Oct 2024
  3. Primary completion18 Mar 2027 (estimated)
  4. Study completion30 Sep 2027 (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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
One group will receive myo-inositol and selenium and one group will not be treated
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06736015
Sponsor's protocol ID
RS39/IRE/23(2869)
Acronym
MYOSEL
Status last verified
Aug 2026
First submitted
5 Dec 2024
Last updated
26 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: At the end of the study, anonymized patient data will be shared on garrbox.it repository

Questions about this trial

What is this clinical trial studying?

A study testing Myo-Inositol 600 mg + Selenium 83 mcg in people with Thyroid Nodule, run by Regina Elena Cancer Institute 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 5 inclusion and 3 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: looking for participants now, as of the sponsor's last update on 26 Aug 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?

Contact Marialuisa Appetecchia, MD (0039 0652666026, marialuisa.appetecchia@ifo.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Evaluation of differences in elastosonography after six months in patients treated with selenium and myo-inositol and patients not treated (controls) (time frame: 6 months). 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 26 Aug 2026.

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