A randomised controlled study In women undergoing an induction of labour to determine if the rate of intravenous fluid used impacts upon the duration of labour
Not Applicable
Recruiting
- Conditions
- Induction of labourReproductive Health and Childbirth - Childbirth and postnatal care
- Registration Number
- ACTRN12621001298808
- Lead Sponsor
- Dr Darren Lowen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
Pregnant women of 37 weeks or greater gestational age, with a single pregnancy in a cephalic presentation who require an induction of labour
Exclusion Criteria
Age < than 18 years
Inability to consent
Augmentation of labour, rather than induction of labour
Pre-eclampsia
Previous caesarean section
Multiple pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method