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A Comparison of the lateral and modified Oxford positions for performing combined spinal epidural anesthesia for Cesarean sectio

Not Applicable
Recruiting
Conditions
Pregnancy, childbirth and the puerperium
Registration Number
KCT0000583
Lead Sponsor
Hallym University Medical Center-Kangnam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
44
Inclusion Criteria

Must satisfy the following two criteria
1. Expectant women at least 38 weeks pregnant scheduled for Caesarean section under combined spinal epidural anesthesia
2. ASA (American Society of Anesthetists) Physical Classification Grade 1 or 2

Exclusion Criteria

1. Preeclampsia
2. Gestational diabetes
3. Intrauterine growth retardation
4. Multiple pregnancy
5. Weighing under 50kg or over 100kg
6. Under 150cm or over 180cm in height
7. Contraindicated for local anesthesia (Lack of consent, local infection at the spinal injection site, coagulopathy)

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
sensory block level
Secondary Outcome Measures
NameTimeMethod
Hemodynamic variables (Blood pressure, Heart rate);Amount of time needed for the sensory block to reach thoracic level 5;Incidence of nausea/vomiting;Amount of ephedrine;Interval between subarachnoid injection and first incision;Interval between subarachnoid injection and end of operation;Maximum level of sensory block and amount of time required;Interval between achievement of maximum level of sensory block and descent of sensory block two levels below;Amount of time required for sensory block to descent to thoracic level 10;Apgar score (at 1 and 5 minutes)
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