Randomised trial of carbetocin versus oxytocin for the prevention of postpartum haemorrhage after caesarean section - LOXY Trial
Phase 1
- Conditions
- Postpartum haemorrhage after caesarean section
- Registration Number
- EUCTR2005-002812-94-GB
- Lead Sponsor
- orth Bristol NHS Trust
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Not specified
- Target Recruitment
- 380
Inclusion Criteria
Women undergoing elective or emergency caesarean section after 37 weeks of pregnancy.
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
Women with multiple gestation, placenta praevia and placental abruption.
Women undergoing caesarean section with general anaesthesia.
Women with caesarean section at less than 37 weeks.
Women having emergency caesarean section for fetal or maternal distress.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method