Title

IV vs IM Oxytocin in the Third Stage of Labor for Prevention of Postpartum Hemorrhage
Intravenous and Intramuscular Administration of Oxytocin in the Third Stage of Labor for Prevention of Postpartum Hemorrhage
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    oxytocin ...
  • Study Participants

    653
The study will evaluate whether prophylactic oxytocin administered in the third stage of labor via IV infusion results in a lower mean blood loss compared to IM injection.
The study will compare the effect of IV infusion and IM oxytocin administration on the proportion of women who experience blood loss greater than or equal t 350 ml, the proportion of women who experience blood loss greater than or equal to 500 ml, side effects, adverse events and change in hemoglobin pre- to post-delivery. It will also assess whether a bleeding history questionnaire can identify women at risk for excessive bleeding and help to define the distribution of bleeding scores among women with and without excessive bleeding.
Study Started
May 31
2012
Primary Completion
Nov 30
2012
Study Completion
Dec 31
2012
Last Update
Mar 28
2016
Estimate

Drug Oxytocin

10 IU oxytocin in 500 ml infusion

Drug Oxytocin

10 IU oxytocin IM injection

IV infusion Active Comparator

Oxytocin 10 IU will be administered IV infusion according to randomization assignment as soon as possible after delivery of the baby.

IM Injection Active Comparator

Oxytocin 10 IU will be administered IM according to randomization assignment as soon as possible after delivery of the baby.

Criteria

Inclusion Criteria:

All women who present in active labor for a live birth at the study hospital will be considered for participation in the study

Exclusion Criteria: Women who are:

Planned or transferred for delivery via Cesarean section
Not delivering a live birth
Unable to provide informed consent due to mental impairment, distress during labor or other reason
Unwilling and/or unable to respond to questionnaires about background characteristics and/or bleeding history.
No Results Posted