Comparison of Prophylactic Norepinephrine and Phenylephrine Infusion for Hemodynamic Effects in Patients With Preeclampsia During Cesarean Section: a Randomized, Controlled Trial
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of this study is to investigate the maternal cardiac output response to prophylactic norepinephrine and phenylephrine infusion for postspinal anesthesia hypotension in parturients with preeclampsia undergoing cesarean section.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 45
Healthy Volunteers: f
View:
• 18-45 years
• Primipara or multipara
• Singleton pregnancy ≥32 weeks
• American Society of Anesthesiologists physical status classification II to III
• Scheduled for cesarean section under spinal anesthesia
Locations
Other Locations
China
General Hospital of Ningxia Medical University
RECRUITING
Yinchuan
Contact Information
Primary
Xinli Ni, Dr.
xinlini6@nyfy.com.cn
86-951-674-3252
Backup
Yi Chen, M.D.
czzyxgp@163.com
86-951-674-3252
Time Frame
Start Date: 2024-02-01
Estimated Completion Date: 2025-04-21
Participants
Target number of participants: 72
Treatments
Active_comparator: Phenylephrine group
Phenylephrine infusion simultaneous with spinal anesthesia
Experimental: Norepinephrine group
Norepinephrine infusion simultaneous with spinal anesthesia
Related Therapeutic Areas
Sponsors
Leads: General Hospital of Ningxia Medical University