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Prediction of Platelet Function Using Viscoelastic Test (ROTEM® Sigma) in Obstetric Anesthesia.

Recruitingn/aAges 18 Years - anyFemaleNicolas Brogly
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In plain words

What the trial is, and whether it could suit you

This prospective observational, non-interventional, single-center study aims to evaluate whether the viscoelastic parameter PLTEM, derived from ROTEM® sigma testing (EXTEM-A5 minus FIBTEM-A5), can accurately estimate platelet count in obstetric patients with thrombocytopenia and/or severe postpartum hemorrhage. The study will include pregnant women older than 18 years managed during labor and delivery at the Hospital General Universitario Gregorio Marañón, Madrid (Spain). The primary objective is to validate the clinical usefulness of PLTEM as a rapid point-of-care tool to support clinical decision-making regarding neuraxial anesthesia and transfusion management in obstetric emergencies.

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📋 Eligibility rules (as published)
Inclusion criteria: * Parturients with a suspicion or confirmed thrombocytopenia before delivery (platelet count \< 120x10\^9/L), * Parturients with severe postpartum haemorrhage (blood loss \>1500 mL) with a suspicion of thrombocytopenia. Exclusion criteria: * parturient age under 18 years; * refusal to participate
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What it tests

  • No Intervention: Observational Cohort
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Where

1 site
Hospital General Universitario Gregorio Marañón
Madrid, Spain
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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