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NCT06033183Recruiting

Integrative Molecular Analysis of Individual Radiosensitivity in Pediatric Oncology

Source: ClinicalTrials.gov · Last updated 22 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Analysis of the individual radiosensitivity in pediatric oncology

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
25 Aug 2023
Start date
2 Dec 2023
Primary completion date
30 Aug 2027
Lead sponsor
Neolys
NCT number
NCT06033183

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 2 Dec 2023 to the primary completion date, 30 Aug 2027
  • 2 sites 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.

Prior treatment

  • Patients with contraindications to radiotherapy
  • Palliative radiotherapy
  • Patient with previous RT treatment in the same area (re-irradiation)

Other

  • Patients with contraindications to blood sampling
  • Patient with an indication of hypofractionated RT
  • Patient follow-up not possible
  • Persons deprived of liberty or under guardianship (including curatorship)
  • \-

Who the study is looking for

  • Minor patient treated for a brain tumor, Ewing tumor, malignant mesenchymal tumor, neuroblastoma, nephroblastoma, Hodgkin's lymphoma treated with radiotherapy (+/- chemotherapy) for curative purposes.
  • Children or adolescents \> 3 years old and \< 18 years old
  • Patient with an indication for radiotherapy as part of the primary tumor local control strategy
  • Theoretical indication for radiotherapy in standard fractionation (1.8 Gy to 2.2 Gy / fraction: 5 fr/week) whatever the technique and the particle used
  • Patient affiliated with a social security scheme
  • Patient and/or parents or holders of parental authority having dated and signed an informed consent

Age in the registry: 3 years to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Centre François Baclesse
Coordinator of this site? Confirm its status
CaenFranceRecruiting
Centre Oscar Lambret
Coordinator of this site? Confirm its status
LilleFranceNot yet recruiting

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