Clinical Trials Directory

Trials / Completed

CompletedNCT00973791

Fluid Management for Cesarean Section II

Fluid Management for Cesarean Section Undergoing Spinal Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
860 (actual)
Sponsor
Nanjing Medical University · Academic / Other
Sex
Female
Age
21 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Fluid management plays an essential role in cesarean section. In previous study (NCT00488111) the investigators found that prior-epidural anesthesia fluid management produced a more significant role in stabilizing the blood pressure and better prognosis after cesarean delivery than that of the posterior-anesthesia ones. Given epidural anesthesia has a time interval before reaching the best state of anesthesia, so the fluid management also has a relatively adequate time to resuscitation. In reality, spinal anesthesia is used popularly except for the epidural anesthesia, whereas spinal anesthesia would produce more significant fluctuation of the hemodynamics compared with the latter. Herein the investigators proposed whether the prior-spinal anesthesia fluid management also produced similar effect on hemodynamic characteristics to the epidural anesthesia.

Conditions

Interventions

TypeNameDescription
DRUGRinger's LactateRinger's Lactate 8 ml/kg was given intravenously before or after spinal anesthesia in cesarean section
DRUGSix percent hydroxyethyl starchHydroxyethyl starch (6%) was given before or after spinal anesthesia in cesarean section

Timeline

Start date
2008-10-01
Primary completion
2009-05-01
Completion
2009-05-01
First posted
2009-09-09
Last updated
2009-09-09

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00973791. Inclusion in this directory is not an endorsement.