Clin2
NCT07052266Likely a fitRecruiting

Combined genetic screening for pregnancy and cancer risk

Hereditary Cancer Syndromes

Part of Cancer, Genetic & congenital clinical trials.

This trial offers a combined genetic test for both common inherited conditions and hereditary cancer risks to pregnant women or those planning pregnancy. It aims to see if adding cancer screening to routine pregnancy testing is helpful.

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

Phase
N/A
Enrollment
550 people
Ages
18 years to 55 years
Study type
Interventional

Who can take part

  • You are between 18 and 55 years old
  • You are pregnant or planning to become pregnant
  • You are getting care at a Weill Cornell Medicine clinic
  • You have chosen to have carrier screening as part of your pregnancy care
  • You have not already had a comprehensive genetic test for hereditary cancer
  • You do not have a blood cancer or a condition that can turn into blood cancer

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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