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This study is a patient registry of people with Desmoplastic Small Round Cell Tumor (DSRCT). A patient registry is a collection of health information about a group of people, and it is usually focused on a specific diagnosis or disease.
The purpose of this registry is to create a database- a collection of information-or better understanding DSRCT. Researchers will use the information from this database to learn more about DSRCT and for current and future research on DSRCT.
Enrollment
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Volunteers
Inclusion criteria
Exclusion criteria
250 participants in 1 patient group
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Central trial contact
Shakeel Modak, MD; Emily Slotkin, MD
Data sourced from clinicaltrials.gov
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