Clin2
NCT04982744Possibly a fitRecruiting

Li-Fraumeni and related syndrome patient registry

Li-Fraumeni SyndromeLi-Fraumeni-Like Syndrome

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

This is a research registry that collects information from people who have Li-Fraumeni or similar inherited cancer syndromes. It helps doctors better understand these conditions and improve future care.

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

Phase
N/A
Enrollment
200 people
Ages
Any age
Study type
Observational

Who can take part

  • You must have a diagnosis of Li-Fraumeni syndrome or a Li-Fraumeni-like syndrome
  • You may need to share personal and medical history for research tracking

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.

Similar studies

Other trials that look related to this one.

NCT01443468Recruiting
Study of Li-Fraumeni syndrome family cancer risk

This study collects medical and genetic information to better understand how often cancer develops in people with Li-Fraumeni syndrome and related family risks. It may help families and doctors plan earlier awareness and follow-up over a person’s lifetime.

Bethesda, Maryland
NCT04541654Recruiting
Study of families with TP53 gene changes in Li-Fraumeni syndrome

This study is looking at how people in families with certain TP53 gene changes (including Li-Fraumeni syndrome) develop health problems over time. It may help doctors better understand risk and improve care for affected families.

Boston, Massachusetts
NCT04367246Recruiting
TP53 (Li-Fraumeni) family biobank and sample study

This study collects and stores health information and biological samples from people who have a known TP53 change (Li-Fraumeni syndrome) and from close family members. The goal is to help researchers learn more about risks and future treatments for this genetic condition.

Philadelphia, Pennsylvania
NCT07005297Not yet recruiting
Genetic Cancer Risk Screening Survey

This study screens people who may have an inherited risk for certain cancers due to their personal or family medical history or known gene changes. By completing a survey, you can help researchers find the right study for you and learn more about your cancer risk.

Rockville, Maryland
NCT03176836Enrolling by invitation
TP53 mutation imaging study for Li-Fraumeni syndrome

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.

Toronto, Ontario
NCT07519356Recruiting
Registry for blood and lymph node disorders

This study collects information from patients with lymphoproliferative disorders—conditions affecting blood and lymph cells—to help doctors better understand these diseases and improve care. Your medical records and information may be used to support research that could benefit future patients.

Pavia, Lombardy

Hear when a new Li-Fraumeni Syndrome trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.