RecruitingNCT07381959

Biomarkers of Brain Injury in Children With Brain Tumors

Biomarkörer för hjärnskada Hos Barn Med hjärntumör


Sponsor

Uppsala University

Enrollment

560 participants

Start Date

Aug 1, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this observational study is to identify biomarkers of treatment-induced brain injury in children treated for primary brain tumors. The main question it aims to answer is: Can investigators identify sensitive plasma biomarker(s) of treatment-induced brain injury in children with primary brain tumors? Researchers will compare results between different treatment modalities (surgery, chemotherapy, radiation versus radiation-naive) and a healthy age- and sex-matched control population, to identify treatment-specific biomarkers. Participants will provide plasma samples at the following time points: before surgery, 1-2 weeks after surgery, as well as at 3-, 6-, 12-, 18-, 24-, and 36 months after surgery. Participants who receive radiation treatment will also provide plasma samples before and during treatment (approximately every 2 weeks). Where possible, plasma samples are also collected before the start of any new treatment (e.g., chemotherapy). Healthy controls will provide samples once.


Eligibility

Max Age: 17 Years

Plain Language Summary

Simplified for easier understanding

This study is looking at blood and fluid markers that can detect brain injury in children with brain tumors in Sweden. Researchers want to understand how radiation and other cancer treatments affect the developing brain by tracking these biomarkers over time. There are three groups: children receiving radiation, children receiving other treatments (no radiation), and healthy children for comparison. **You may be eligible if...** - You are a child aged 0–17 years old - You have been diagnosed with a primary brain tumor at a Swedish university hospital - You are being treated with or without radiation at Skandion Clinic or another hospital in Sweden - OR you are a healthy child aged 0–17 with no chronic illness (for the control group) **You may NOT be eligible if...** - Your tumor is only in the spinal cord - Your tumor has been classified as palliative (end-stage) from the start, such as certain brainstem tumors - You have a chronic disease requiring ongoing medication (control group only) - There are language barriers preventing you from giving informed consent Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Uppsala University

Uppsala, Sweden

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NCT07381959


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