A study to determine the cardiovascular effects of different methods of administering the oxytocic drug Syntocino
Completed
- Conditions
- Pregnancy and Childbirth: AnaesthesiaPregnancy and ChildbirthAnaesthesia
- Registration Number
- ISRCTN07452238
- Lead Sponsor
- Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 30
Inclusion Criteria
Women choosing spinal anaesthesia for elective Caesarean:
15 in control group receiving syntocinon 5 units intravenously (IV) as a bolus after delivery 15 in study group receiving syntocinon 5 units IV continuously over 5 min after delivery
Exclusion Criteria
Not provided at time of registration
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method