Actively Recruiting

All Genders
NCT03609112

Neurocognitive Risks in Children With Solid Tumors

Led by Gustave Roussy, Cancer Campus, Grand Paris · Updated on 2024-12-13

1000

Participants Needed

1

Research Sites

569 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The survival rate of children with cancer has improved significantly in recent years thanks to the progress of different therapies. The neurocognitive sequelae related to treatments and illness are more or less well known. Four factors seem to be associated with neurocognitive sequelae: treatment, the tumor itself, environmental factors like the socio-economic status of parents and biological factors. Main purpose of the study is to establish a score to assess the risk of neurocognitive sequelae in these children based on these factors (treatment, tumor, and environmental factors)

CONDITIONS

Official Title

Neurocognitive Risks in Children With Solid Tumors

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged 6 to 16 years and 11 months during the study period
  • Diagnosis of a solid tumor
  • Treatment and follow-up at Gustave Roussy
  • Minimum 6 months since end of initial treatment for patients not treated with methotrexate
  • No minimum time since treatment for patients treated with methotrexate
  • Parental or legal representative non-opposition obtained
  • Affiliated to a social security scheme
Not Eligible

You will not qualify if you...

  • Patients with other pathologies linked to mental retardation such as autism or genetic syndromes
  • Patients lost to follow-up
  • Deceased patients
  • Patients treated for pathologies with very short-term prognosis (e.g., infiltrating brainstem glioma, recurrence during treatment)
  • Non-French speaking patients

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Gustave Roussy

Villejuif, Val De Marne, France, 94805

Actively Recruiting

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Research Team

C

Christelle DUFOUR, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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