Clin2
NCT03176836Possibly a fitEnrolling by invitation

TP53 mutation imaging study for Li-Fraumeni syndrome

Li-Fraumeni Syndrome

Part of Cancer, Genetic & congenital, Hormones & metabolism clinical trials.

This study takes special body images (MRI) in people from families with Li-Fraumeni syndrome, especially those who carry a TP53 gene mutation. The goal is to see whether MRI can help spot problems earlier in a higher-risk group.

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

Phase
N/A
Enrollment
30 people
Ages
Up to 18 years
Study type
Interventional

Who can take part

  • You’re from a family with Li-Fraumeni syndrome (LFS).
  • You have a known TP53 mutation, or you are required to carry that mutation in your family.
  • You can safely have an MRI scan (no unsafe metal/implants for MRI).
  • You don’t have an implanted device or prosthesis that can be affected by the MRI magnet (for example, certain pacemakers or metal fragments).
  • You can tolerate the MRI room even if you feel anxious in small spaces (claustrophobia should be manageable).

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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