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2024-512642-42-00RecruitingPhase 3

Randomized study to protect from radiation iatrogenic hypothyroidism patients with medulloblastoma (any stage, any biological risk) and pediatric patients with Hodgkin lymphoma and non-Hodgkin lymphoma needing radiation therapy on thyroid site - WINHYPO 2021

Source: EU CTIS (euclinicaltrials.eu) · Last updated 23 Sept 2026

Next steps

Brief summary (registry, in English)

To evaluate if the incidence of hypothyroidism after radiation therapy in medulloblastoma, Hodgkin and non-Hodgkin lymphomas can be reduced by TSH suppression during irradiation.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
65 (estimated)
First submitted
18 Mar 2024
Start date
13 Dec 2021
Lead sponsor
Fondazione IRCCS Istituto Nazionale Dei Tumori
EU CT number
2024-512642-42-00
EudraCT number
2021-001385-38

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 65
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for people with medulloblastoma, Hodgkin lymphoma or non-Hodgkin lymphoma who are about to have radiotherapy that includes the thyroid gland, and who have no earlier thyroid underactivity.

Sex
All sexes can join.
Disease stage
Medulloblastoma (any stage, any biological risk), Hodgkin lymphoma or non-Hodgkin lymphoma. Radiotherapy planned to include the thyroid gland tissue.
Earlier treatment
Must not yet have had radiotherapy that included the thyroid gland. Must not have had thyroid underactivity (primary or secondary hypothyroidism) before.

Main reasons for not taking part

  • Radiotherapy including the thyroid gland already given
  • Previous primary or secondary hypothyroidism
  • No signed consent

Read by machine on 9 Nov 2026.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any patient with medulloblastoma, Hodgkin/non-Hodgkin Lymphoma after radiotherapy including thyroid parenchyma;

Other

  • Not signed consent.

Who the study is looking for

  • Any patient with medulloblastoma, Hodgkin/non-Hodgkin Lymphoma BEFORE RADIOTHERAPY (RT) PLANNING INCLUDING THYROID PARENCHYMA without previous primary or secondary hypothyroidism;
  • Written informed consent prior to any study-specific analysis and/or data collection.

Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Fondazione IRCCS - Istituto Nazionale dei TumoriMilanItalyRecruiting

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This page is information, not medical advice. Discuss any trial with your doctor.