Could Pre-operative Rectal Misoprostol Reduce Intra-operative Blood Loss During Ceserean Section?
Sponsored by Ain Shams University
About this trial
Last updated 9 years ago
Study ID
POMCS
Status
Completed
Type
Interventional
Phase
Phase 2/Phase 3
Placebo
No
Accepting
18 to 40 Years
Female
Not accepting
Healthy Volunteers
Trial Timing
Ended 9 years ago
What is this trial about?
- Misoprostol reduces the uterine bleeding after cesarean delivery without harmful effects
on either mother or baby.
- The aim of the this study is to address if there is any benefits 'regarding the
intra-operative blood loss' from preoperative rectal administration of 400 mic of
Misoprostol in addition to the routinely administrated 10 units of oxytocin
What are the participation requirements?
Inclusion Criteria
- 38-41 weeks of amenorrhea
- scheduled for elective lower segment cesarean section
Exclusion Criteria
- confirmed intrauterine fetal death
- more than previous 2 ceserean sections
- multiple pregnancy
- antepartum haemorrhage
- self-reported maternal heart disease
- current diagnosis of severe malaria or acute bacterial infection