A prospective trial to determine if we can reduce the amount of vasopressor for prevention of hypotension caused by spinal anesthesia when ondansetron is administered before spinal anesthesia for cesarean sectio
Not Applicable
- Conditions
- Pregnancy, childbirth and the puerperium
- Registration Number
- KCT0003609
- Lead Sponsor
- Bundang CHA General Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- 142
Inclusion Criteria
Singleton Korean patients between the age of 19 and 50 years of American Society Anesthesiologists (ASA) physical status II scheduled for elective caesarean section.
Exclusion Criteria
foreigner, QTc prolongation on electrocardiogram, contraindication to neuraxial block, BMI >45kg/m2, preexisting hypertension or pregnancy induced hypertension requiring treatment, placenta previa, abruptio, allergic to the medicine,gestational ages< 35 wks,intrauterine growth retardation, fetal distress, cardiac/renal or other end-organ disease,patients in active labor.
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method dose of infused phenylephrine during Cesarean delivery
- Secondary Outcome Measures
Name Time Method incidence of hypotension;incidence of bradycardia (<60 bpm);incidence of intraoperative nausea and vomiting;incidence of shivering