Actively Recruiting

Phase Not Applicable
Age: 12Years - 36Years
All Genders
NCT06517927

Prevalence of Long-term Dental Effects of Chemotherapy in Childhood Cancer Survivors Diagnosed With Cancer Before the Age of 10

Led by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Updated on 2024-11-19

142

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To date, there are no methods for assessing the risk of oral developmental defects that could predict long-term adverse effects in childhood cancer survivors. Having such a method at our disposal would enable us to better assess the risk to develop those defects and will help us provide new prevention and treatment strategies to ensure a healthy oral development. The aims of this study are : * Assess the caries risk in childhood cancer survivors compared with a control group. * Assess the dental development defects risk in childhood cancer survivors compared with a control group.

CONDITIONS

Official Title

Prevalence of Long-term Dental Effects of Chemotherapy in Childhood Cancer Survivors Diagnosed With Cancer Before the Age of 10

Who Can Participate

Age: 12Years - 36Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with cancer before age 10 (for childhood cancer survivors group)
  • Treated with chemotherapy (for childhood cancer survivors group)
  • At least 12 years old at the time of the study follow-up appointment
Not Eligible

You will not qualify if you...

  • Diagnosed and treated for cancer after age 10
  • Younger than 12 years old at study recruitment
  • Having syndromes or diseases that affect teeth
  • Pregnant patients
  • Refusal or inability to undergo dental and radiographic examination

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

Cliniques universitaires Saint-Luc

Brussels, Belgium, 1200

Actively Recruiting

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Research Team

A

Armand IRAKOZE

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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