The purpose of the study is to assess the coagulation changes that occur in laboring patients
undergoing non-elective (intrapartum)Cesarean delivery using thromboelastography (TEG). We
will compare coagulation data to assess potential coagulation changes associated with
hemoglobin changes before and after surgery, and related to estimated blood loss.
Stanford is currently not accepting patients for this trial.
For more information, please contact Alexander J Butwick, MBBS, FRCA, (650) 736 - 8513.
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