EUCTR2005-001361-34-GB
Active, not recruiting
Phase 1
A randomised controlled trial of oxytocin 5 IU versus oxytocin 5 IU and 30 IU infusion for the control of blood loss at elective caesarean section - pilot study. - caesarean third stage trial
niversity of Dundee0 sites75 target enrollmentMarch 31, 2005
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversity of Dundee
- Enrollment
- 75
- Status
- Active, not recruiting
- Last Updated
- 9 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Healthy women at term (\> 36 weeks) with a singleton pregnancy booked for an elective caesarean section
- •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
- •placenta praevia; multiple pregnancy; known coagulopathy; current anti\-coagulant therapy; thrombocytopenia
Outcomes
Primary Outcomes
Not specified
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