MedPath

Extending low-dose epidural for emergency Caesarean section - a comparison of bicarbonated lidocaine with 0.5% levobupivacaine

Conditions
/A
Registration Number
EUCTR2006-001033-18-GB
Lead Sponsor
Chelsea and Westminster Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
Female
Target Recruitment
100
Inclusion Criteria

Inclusion criteria will be established labour beyond 36 weeks gestation and women requesting an epidural for pain relief in labour.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Exclusion critera will be an epidural top-up of solution stronger than bupivacaine 0.1% within the previous hour, pehtidine in the last 4 hours, multiple preganct, pre-eclampsia, antepartum haemmorage, cardiac disease, any contra-indication to regional analgesia or anaesthesia and any allergy to non-steroidal anti-inflammatory drugs

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath