oxygen perfusion from saturation probe as a index of hypotension following spinal anesthesia in elective caesarean surgery
Not Applicable
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2023/03/050192
- Lead Sponsor
- DR NETHRA S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I and II
BMI <= 40 kg/m²
gestational age between 36 â?? 40 weeks
Exclusion Criteria
Unwilling to participate in the study
Contraindications to regional anesthesia
Those requiring emergency caesarean section
Pregnancy induced hypertension or preeclampsia
Gestational diabetes mellitus
Twin gestation, placenta previa
BMI >= 40, blood loss > 1000 ml
Failure to achieve sensory block to T6 dermatome
Gestational age <36 or >40 weeks
Cardiovascular or cerebrovascular disease
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine whether baseline perfusion index can be used to predict hypotension following <br/ ><br>spinal anesthesia for the elective lower segment caesarean delivery. <br/ ><br>Timepoint: within a minute after attaching pulse oximeter(baseline) <br/ ><br>
- Secondary Outcome Measures
Name Time Method nilTimepoint: nil