Clin2
NCT04788927Possibly a fitNot yet recruiting

Predicting spread risk in pheochromocytoma and paraganglioma

ParagangliomaPheochromocytomaGenetic Predisposition to DiseasePathologySomatic MutationHead and Neck CancerNeuroendocrine Tumors

Part of Cancer clinical trials.

This study looks at past patient data to find patterns that might predict whether a pheochromocytoma or paraganglioma (rare tumors of the adrenal glands or nerve tissue) will spread. It aims to create a tool to help doctors estimate risk and plan treatment.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
400 people
Ages
birth to 120 years
Study type
Observational

Who can take part

  • You must have been diagnosed with a pheochromocytoma or paraganglioma (or a genetic variant that increases risk for these tumors).
  • Your diagnosis must have been made in Denmark since 1996.
  • You must have tumor tissue or blood samples stored in a biobank for the study to use.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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