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Misoprostol Before and After Cesarean Section

The Effect of Misoprostol Given Preoperative Versus Postoperative on Blood Loss With Elective Cesarean Section: Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03463070
Enrollment
140
Registered
2018-03-13
Start date
2018-03-31
Completion date
2018-09-30
Last updated
2018-03-13

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

Conditions

Post Partum Hemorrhage

Keywords

misoprostol, postpartum haemorrhage

Brief summary

comparison of the effect of misoprostol before and after cesarean on the blood loss

Detailed description

70 women who received 600 mg misoprostol rectally preoperatively versus 70 women who received 600 mg misoprostol postoperatively at operating theatre

Interventions

DRUGrectal misoprostol 600mg

70 women who received 600 mg misoprostol postoperatively at operating theatre

Sponsors

sarah mohamed hassan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Women not in active labor have reactive non-stress test. * No contraindications to prostaglandins. * Have no history of coagulopathy.

Exclusion criteria

* Placenta previa. * Maternal hypertension. * Diabetes mellitus. * Previous CS and those with active labor. * Multiple Fibroid uterus. * Multiple pregnancies or polyhydramnios. * Previous myomectomy, previous history of PPH.

Design outcomes

Primary

MeasureTime frameDescription
intraoperative blood lossthe operation timeDifference in weight of linen towels (gm)+Volume of contents of suction bottle (ml)
postoperative blood lossevery 6 hours during first 24 hours.weighing the soaked napkins after collection of soaked towel

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026