New study to track recovery in kids with brain tumors
NCT ID NCT07315230
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will follow 30 children under 18 who have surgery for a specific type of brain tumor (midline posterior fossa tumors). The goal is to see how well they recover and what factors affect their recovery and survival. The results may help doctors better predict outcomes and personalize treatment for these young patients.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
Pediatric patients younger than 18 years presenting to the Neurosurgery Department, Assiut University Hospital, with radiologically confirmed midline posterior fossa brain tumors and considered candidates for surgical resection. Participants are recruited consecutively from routine clinical care and followed postoperatively for functional and radiological outcomes.
- Ages
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0 to 17 years
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients less than 18 years old * patient with midline posterior fossa tumors * patient is fit for surgery Exclusion Criteria: * patinent older than 18 years old * patients with non-midline posterior fossa or other brain tumors. * patient is unfit for surgery . * Incomplete Data: Missing essential study data. * Secondary Malignancy: Metastatic disease.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.