No registrations found.
ID
Source
Brief title
Health condition
C-section, Chloroprocaine, intrathecal, Bupivacaine, caesarean, Sufentanil, Ampres, Marcaine.
Sponsors and support
Laarbeeklaan 101
1090 Jette
Laarbeeklaan 101
1090 Jette
Intervention
Outcome measures
Primary outcome
Earlier releave of motor block (less then 90' after injection).
Secondary outcome
N/A
Background summary
Evaluation of the use of Chloroprocaine (and Sufentanil) during C-section and its effects on sensory and motor block.
Study objective
The goal of this trial is to investigate the efficacy of the IMP during c-section with and without the use of Sufenta: As well as start of action, duration of action, the degree of motor and sensory block as well as the hight of the block itselfs will be investigated.
Study design
End of c-section and final releave of motor block.
Intervention
Measurement of sensory and motor block, hemodynamic monitoring during procedure, feeling of nausea and vomitting, feeling of pain, relief of motor block.
Veerle Mossevelde, van
Brussels 1090
The Netherlands
+32 (0)2 4763134
veerle.vanmossevelde@uzbrussel.be
Veerle Mossevelde, van
Brussels 1090
The Netherlands
+32 (0)2 4763134
veerle.vanmossevelde@uzbrussel.be
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.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL3879 |
| NTR-old | NTR4076 |
| Other | MEC UZ Brussel : 2013/186 |
| ISRCTN | ISRCTN wordt niet meer aangevraagd. |