Phenylephrine infusion for prevention of hypotension during spinal anesthesia for elective cesarean sectio
Not Applicable
- Conditions
- elective caesarean section
- Registration Number
- JPRN-jRCTs041190070
- Lead Sponsor
- akashima Daiki
- Brief Summary
46 participants were enrolled into this study. The frequency of hypotension, the primary endpoint, was significantly lower in the phenylephrine group than in the conventional group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 46
Inclusion Criteria
1.elective caesarean section under spinal anesthesia
2.age over 20 years old
3.written informed consent
Exclusion Criteria
1.cannot communicate
2.patients complicated with hypertension, heart and vessel disease, diabetes
3.multiple pregnancy, excessive amniotic fluid, fetal stunt
4.patients whose BMI >35
5.patients who are considered to be inappropriate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method