New radiation approach aims to tame pituitary tumors with fewer side effects
NCT ID NCT06826170
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new way of delivering radiation for people with non-secreting pituitary adenomas that came back or remained after surgery. Instead of a single high dose, the radiation was given in five smaller daily doses. The goal was to see if this approach could control tumor growth while reducing damage to nearby nerves and the pituitary gland. Twenty-five patients were followed for at least a year with MRI scans, eye tests, and hormone checks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hypofractionated stereotactic radiotherapy (radiation therapy given in 5 daily sessions)
- What this could lead to
- If successful, this approach could offer a safer way to treat residual or recurrent pituitary tumors with fewer side effects on vision and hormone function.
- What could go wrong
- This is a small, early-phase study with only 25 participants. It may not confirm long-term safety or effectiveness, and some patients may still experience side effects or tumor progression.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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25 people
The number who actually took part.
- Started
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Sep 2020
- Finished
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May 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Residual or progressive non secreting pituitary adenoma; * Exclusion of other treatment approach (second surgery, wait and scan; suppressive therapy) by a multidisciplinary team * Age ≥ 18 years; KPS ≥ 70 * Written privacy consent; * Ability to give informed consent; Exclusion Criteria: * Previous cranial irradiation; * Diagnosis of secreting adenoma; * pregnancy status; * unable to undergo MRI or CT scans; * unable to give informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Fondazione IRCCS Istituto Neurologico C Besta
Milan, Milan, 20133, Italy
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Other studies related to the condition(s) this trial covers.
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