International Clinical Trial: A comparative study on the optimal infusion rate of continuous infusion of norepinephrine for prevention of hypotension after cesarean section in normal and obese women

Geneva, Jan. 12 -- International Clinical Trials Registry received information related to the study (ChiCTR2500115478) titled 'A comparative study on the optimal infusion rate of continuous infusion of norepinephrine for prevention of hypotension after cesarean section in normal and obese women' on Dec. 26, 2025.

Study Type: Interventional study

Study Design: Parallel

Primary Sponsor: Women's Hospital School of Medicine Zhejiang University

Condition: parturients who are scheduled for elective cesarean delivery

Intervention: Normal group 1:Intravenous prophylactic infusion of norepinephrine 0.02 µg/kg/min Normal group 2:Intravenous prophylactic infusion of norepinephrine 0.03 µg/kg/min Normal group 3:Intravenous prophyl...