Randomised comparative trial of Bupivacaine and 2-Chloroprocaine by caesarean section.
- Conditions
- C-section, Chloroprocaine, intrathecal, Bupivacaine, caesarean, Sufentanil, Ampres, Marcaine.
- Registration Number
- NL-OMON22342
- Lead Sponsor
- Z BrusselLaarbeeklaan 1011090 Jette
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
All healthy(ASA I-II) women with an uncomplicated singleton pregnancy between 18-40 y undergoing a planned caesarian.
Pregnancy > or equal to 37 weeks.
Exclusion Criteria
Women who belong to ASA III-IV classification, BMI >35, length <150 cm, foetus with known fetal abnormality, pregnancy less than 37 weeks, known allergy for the used local anesthetics and (pre) eclampsia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Earlier releave of motor block (less then 90' after injection).
- Secondary Outcome Measures
Name Time Method