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NCT06726642Possibly a fitRecruiting

Blood test study for people with inherited cancer risk

Hereditary Cancer Syndrome

Part of Cancer, Digestive system, Genetic & congenital, Hormones & metabolism, Skin, Women’s health & pregnancy clinical trials.

This study looks for DNA fragments in blood of people with certain inherited cancer syndromes. It may help find cancer earlier or guide better monitoring. You would give blood samples every 4 months (if in the experimental group).

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

Phase
N/A
Enrollment
1,000 people
Ages
Up to 90 years
Study type
Observational

Who can take part

  • You have a confirmed inherited cancer syndrome (like Lynch, HBOC, NF1, LFS, PALB2, or HDGC).
  • You are already in a regular cancer screening program with your doctor.
  • You do not have a cancer diagnosis or treatment in the last 3 years.
  • You are not being tested currently for a suspected cancer.
  • You can commit to giving a blood sample three times a year.

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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