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A randomised trial of oxytocin bolus versus oxytocin bolus and infusion for the control of blood loss at elective caesarean section. - caesarean blood loss trial

A randomised trial of oxytocin bolus versus oxytocin bolus and infusion for the control of blood loss at elective caesarean section. - caesarean blood loss trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2006-004799-11-IE
Enrollment
Unknown
Registered
2007-03-14
Start date
2007-11-29
Completion date
Unknown
Last updated
2015-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Elective lower segment caesarean section

Interventions

Trade Name: Syntocinon Product Name: Syntocinon Pharmaceutical Form: Concentrate for solution for infusion Pharmaceutical form of the placebo: Solution for infusion Route of administration of the plac

Sponsors

Coombe Women's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion 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) F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Placenta praevia; multiple pregnancy; known coagulopathy; current anti-coagulant therapy; thrombocytopenia

Design outcomes

Primary

MeasureTime frame
Main Objective: To evaluate whether an additional oxytocin infusion reduces blood loss at caesarean section;Secondary Objective: To quantify side effects of an oxytocin infusion at caesrean section;Primary end point(s): Estimated mean operative blood loss; use of additional uterotonic agent; incidence of side effects

Countries

Ireland

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026