The effect of goal directed fluid, inotrope and vasopressor therapy in preeclamptic patients undergoing caesarean section delivery under spinal anaest
Not Applicable
Not yet recruiting
- Conditions
- Pregnancy and ChildbirthSurgery
- Registration Number
- PACTR201604001597634
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Pregnant patients, 18 years of age and older, with the diagnosis of preeclampsia (as per the attending obstetrician), undergoing caesarean section delivery under spinal anaesthesia will be included in the study.
Exclusion Criteria
Patients:
-with fetal distress
-unable to give informed consent (including failure to understand explanation of the study in English language)
-who decline to participate
-already on vasopressor therapy prior to arrival in theatre
-with antepartum haemorrhage
-expected to have general anaesthesia
-converted from spinal to general anaesthesia intraoperatively
-where there is deviation from the study protocol
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method