Clinical trial Recruiting at 1 site Observational

Creating a database for pediatric CNS tumors in Asia

Official title: National Cancer Center Korea

Run by National Cancer Center, Korea · NCT05982691 · Data updated 2026-11-12

This study is creating a database to collect information about children with CNS germinoma tumors in Asia to help improve treatment and care for them.

Quick facts

Study typeObservational
SexAll
Enrollment400 (estimated)
SponsorNational Cancer Center, Korea
Government
Locations1 site (Goyang-si, Gyeonggi-do)
StatusRecruiting
StartedAugust 5, 2022
Main results expectedDecember 31, 2028
Study endsDecember 31, 2032
Registry record updatedAugust 8, 2023
Trial IDNCT05982691 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients aged 0 to 40 diagnosed with CNS germinoma who consent to participate in the research.

Probably not a fit

Patients who do not have a diagnosis of CNS germinoma or who do not consent to participate will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to establish an Asian consortium focused on collecting data related to pediatric central nervous system (CNS) tumors, specifically CNS germinoma. The study will begin by registering patients diagnosed with CNS germinoma from 2022 to 2027 and will develop clinical protocols tailored for pediatric CNS tumors in Asia. The consortium will also analyze medical records until 2030 and conduct interim assessments to ensure data quality and integrity. The final analysis of treatment outcomes is projected for 2032.

Why it matters

Potential benefit: If successful, this initiative could enhance understanding and treatment of pediatric CNS tumors in Asia, leading to improved patient outcomes.

How similar studies have gone: While this approach is collaborative and data-driven, similar studies have shown promise in improving treatment protocols for CNS tumors, indicating potential for success.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* A patient who was diagnosed with CNS GCT and agreed to participate in the research between 2022-2027.

  * Patients diagnosed between 2016-2022 can be enrolled if the participating institute has IRB approval for recruiting these patients as separate IRB document (Seoul Asan Hospital) or by comprehensive IRB document (Singapore NCC, Taiwan Medical University), or by recruitment on the basis of acquirement of the consent form for research (NCC, Korea).

    * The age at the time of diagnosis is 0\< ≤40 years

      * A patent who has been diagnosed with the relevant tumor via an operation or a biopsy ⑤ In the case of CNS germinoma, a biopsy may not have been performed on a patient. In this case, the patient may register as germinoma if he or she meets the following criteria: -Germinoma is strongly suspected radiologically, and a tumor marker from serum or cerebrospinal fluid (CSF) has not increased above the institute's reference normal value; -Germinoma is suspected radiologically, and a tumor marker from serum or CSF has elevated above the institute's reference normal value (tumor markers may be AFP or hCG)

Exclusion Criteria:

① The patient or the guardian of the patient did not consent to participate.

Where it's running

  • National Cancer Center, Korea
    Goyang-si, Gyeonggi-do, South Korea
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.