drugset / Trial / NCT02278575

Atenativ Effect on Uterine Blood Flow and Preeclampsia

NCT02278575

NaSingle-groupOpen-labelSupportive care

Summary

The study will be an open controlled pilot study of 6 patients with early-onset severe preeclampsia. Patients will receive Atenativ in addition to conventional therapy The patients will be followed up within the study until three days after delivery. Laboratory analyses and uterine and umbiliacal blood flow will be determined.

Timeline

Start
2016-01
Primary completion
2017-05
Completion
2017-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Atenativ Protein / enzyme biologic Intravenous