Post Partum Hemorrhage Clinical Trial
Official title:
The Effect of Misoprostol Given Preoperative Versus Postoperative on Blood Loss With Elective Cesarean Section: Randomized Controlled Trial
Verified date | March 2018 |
Source | Kasr El Aini Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
comparison of the effect of misoprostol before and after cesarean on the blood loss
Status | Not yet recruiting |
Enrollment | 140 |
Est. completion date | September 2018 |
Est. primary completion date | September 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 35 Years |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
Egypt | Kasr El Ainiy Hospital | Cairo |
Lead Sponsor | Collaborator |
---|---|
sarah mohamed hassan |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | intraoperative blood loss | Difference in weight of linen towels (gm)+Volume of contents of suction bottle (ml) | the operation time | |
Primary | postoperative blood loss | weighing the soaked napkins after collection of soaked towel | every 6 hours during first 24 hours. |
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