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Misoprostol Before and After Cesarean Section

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

Clinical Trial Summary

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

Clinical Trial Description

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

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03463070
Study type Interventional
Source Kasr El Aini Hospital
Contact
Status Not yet recruiting
Phase Phase 3
Start date March 2018
Completion date September 2018
View Details
See also
  Status Clinical Trial Phase
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Active, not recruiting NCT03069859 - Use of TXA to Prevent Postpartum Hemorrhage Phase 2
Not yet recruiting NCT03891082 - A Comparative Study Between Bakri Balloon and B Lynch Suture Used to Control Primary Postpartum Hemorrhage After Cesarean Section N/A
Recruiting NCT05532215 - Sublingual Misoprostol in Reduction of Caesarean Blood Loss N/A
Not yet recruiting NCT06255496 - QStat Cartridge in Obstetric Patients
Completed NCT03907605 - Anti-Mullerian Hormone (AMH) is a Marker for Ovarian Reserve. There Are Many Studies About AMH Changes in Ovarian Surgery, But Little is Known for Other Surgeries. We Seek to Investigate the Hormone Variations Before and After Uterine Artey Ligation for Postpartum Hemorrage (PPH)