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
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.
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.
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 →Regina Elena Cancer Institute is the lead sponsor of 94 studies on the registry; 51 are open to participants now.
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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.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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
Drug page: Inositol
Myo-Inositol 600 mg + Selenium 83 mcg: 1 tablet once a day for 6 months
Also known as: Tiroxil 4.0
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
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
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
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
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
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
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
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.
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.
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Studies of the drug tested here: Inositol
Regina Elena Cancer Institute