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Clinical Trials/EUCTR2005-001361-34-GB
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.

Registry
who.int
Start Date
March 31, 2005
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
niversity of Dundee

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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