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NCT07716579Completed

Assessment of Endocrine and Metabolic Late Effects After Childhood Brain Tumor Treatment

Late Endocrine and Metabolic Consequences of Treatment of Primary Brain Tumors in Childhood

Source: ClinicalTrials.gov · Last updated 13 Aug 2026

Brief summary (registry, in English)

This prospective, single-group interventional study evaluates endocrine and metabolic late effects in survivors of primary brain tumors treated during childhood. According to the study protocol, participants were prospectively assigned to undergo the Study-Specific Endocrine and Metabolic Late-Effects Assessment. The assessment included anthropometric measurements, repeated blood pressure measurements, clinical endocrine evaluation, fasting laboratory testing, and protocol-defined bone and vascular assessments. The purpose of the study was to identify the frequency and severity of endocrine and metabolic late effects and to evaluate their associations with tumor characteristics, previous cancer treatment, age at diagnosis, and physical functioning.

Status (registry)
Completed
Study type
Interventional
Enrollment
12 (actual)
First submitted
15 Jul 2026
Start date
3 Jul 2023
Primary completion date
31 Dec 2025
Lead sponsor
Institute of Oncology Ljubljana
NCT number
NCT07716579

What you commit to

  • Study type: Interventional
  • Participants enrolled: 12
  • From 3 Jul 2023 to the primary completion date, 31 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Failure to meet the inclusion criteria.

Other

  • Absence of written informed consent from the participant or, when applicable, from a parent or legal guardian.

Who the study is looking for

  • Individuals treated for a primary brain tumor in Slovenia between 2008 and 2018 while aged 0 to 18 years.
  • Survival for at least 5 years after the diagnosis of a primary brain tumor.
  • Written informed consent provided by the participant or, when applicable, by a parent or legal guardian.

Age in the registry: 5 years to 35 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institute of Oncology Ljubljana
Coordinator of this site? Confirm its status
LjubljanaSloveniaUnknown status

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