Registry Collecting Information on Children with Cancer in French-Speaking Africa
Collects information on children with cancer treated in African oncology units.
Plain-language title generated from the registry record
Registry title: Hospital Based Registry of Childhood Cancer in Pediatric Oncology Units in French Speaking Africa
Key facts
- Where
- Bamako, MaliSee the site
AI summary: who the study is looking for
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The registry is looking for children and teenagers under 18 with any type of cancer who come for treatment at one of the taking-part units.
- Age
- From 1 Day to 18 Years (less than 18 years of age).
- Sex
- Boys and girls can both join.
- Disease stage
- Any type of cancer.
Main reasons for not taking part
- No cancer found
- Age greater than 18 years
Read by machine on 9 November 2026.
Where in Mali
- CHU Gabriel Touré (HGT)Bamako, MaliContact: Boubacar TOGO, PROFESSEURTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- French Africa Pediatric Oncology Group
- Trial code
- NCT03803735
- Record updated
- 3 October 2025
- Original description
The ultimate aim of this registry is to collect precise information concerning the children coming to oncology units working with the French African Oncology Group. This data will help to plan and provide correct pediatric oncology treatment and care for this population.Read full original descriptionShow less
French African Pediatric Oncology Registry
The ultimate aim of this registry is to collect precise information concerning the children coming to oncology units working with the French African Oncology Group. This data will help to plan and provide correct pediatric oncology treatment and care for this population.
Collecting the data will give much needed information on numbers, stage, treatment and outcome. The register will give data for local and national health authorities in planning pediatric cancer programs.
Inclusion: Any child presenting at any one of the participating units for treatment; Any child with any type of cancer; Any child or adolescent less than 18 years of age.
Exclusion: No cancer found; Age greater than 18 years -.