Clin2
NCT06529042Possibly a fitEnrolling by invitation

Sickle Cell Risk in Pregnancy Tool Study

Sickle Cell DiseasePregnancy, High RiskPregnancy Complications

Part of Blood & lymphatic, Genetic & congenital, Women’s health & pregnancy clinical trials.

This study is developing a risk assessment tool to help predict complications in pregnant women with sickle cell disease. It reviews medical records from women who have received prenatal care and given birth at participating hospitals.

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

Phase
N/A
Enrollment
1,000 people
Ages
16 years to 60 years
Study type
Observational

Who can take part

  • You must be 16 or older.
  • You must have a confirmed type of sickle cell disease (such as HbSS, HbSC, or certain thalassemia combinations).
  • Your pregnancy must have reached at least 16 weeks (and you received care at a participating hospital).
  • Your medical records from pregnancy and birth must be complete and available at that center.

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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