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Clinical Trial Summary

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.


Clinical Trial Description

This register is a registration of all children entering hospital based pediatric oncology units, working in selected hospitals in French speaking Africa. The data collected includes: demographic and socioeconomic status as well as clinical status and outcome. The register also collects information on vital status, treatment abandonment and loss to follow-up. Data, collected locally is entered on line using the Research Electronic Data Capture (REDCap) program. Data are stored under the responsibility of the IT department at Gustave ROUSSY in Paris- Villejuif. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03803735
Study type Observational [Patient Registry]
Source French Africa Pediatric Oncology Group
Contact Brenda MALLON, MSC
Phone + 33142115411
Email brenda.mallon@gustaveroussy.fr
Status Recruiting
Phase
Start date January 1, 2016
Completion date December 2030

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