Clinical trial
DNA Variations in the Gene in Young Patients With Wilms' Tumor
NCT00088803 · Children's Oncology Group, Other · Completed
Key facts
| NCT number | NCT00088803 |
|---|---|
| Title | DNA Variations in the Gene in Young Patients With Wilms' Tumor |
| Official title | The Incidence, Inheritance, and Prognostic Significance of Polymorphisms in the RASSF1A Gene in Children With Wilms Tumors |
| Lead sponsor | Children's Oncology Group, Other |
| Collaborators | National Cancer Institute (NCI) NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Kidney Cancer |
| Intervention type | Genetic |
| Interventions | molecular genetic technique, polymerase chain reaction, polymorphism analysis |
| Enrollment | 471 |
| Start date | Aug 1, 2004 |
| Primary completion | May 1, 2016 |
| First posted | Aug 5, 2004 |
| Last update posted | May 19, 2016 |
| Countries | Australia, Canada, Netherlands, New Zealand, Puerto Rico, Switzerland, United States |
At a glance
- 100–999 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: