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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03366259
Other study ID # 4122017
Secondary ID
Status Not yet recruiting
Phase Phase 2/Phase 3
First received December 4, 2017
Last updated December 7, 2017
Start date December 2017
Est. completion date February 2018

Study information

Verified date December 2017
Source Kasr El Aini Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of our study is to assess the value of administration of prostaglandins before cesarean section to reduce the amount of blood loss


Description:

160 full term pregnant patients candidate for elective cesarean section were randomly allocated into 2 groups ,80 patients will receive 200mcg of rectal prostaglandins before cesarean section and 80 patients are used as control receiving placebo


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 160
Est. completion date February 2018
Est. primary completion date February 2018
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:pregnant patients full term elective cesarean section

Exclusion Criteria:

- medical disorder with pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Misoprostol 200Mcg Tab
administration of 200 Mcg of misoprotol rectal
Procedure:
elective cesarean section
elective cesarean section for full term patients

Locations

Country Name City State
Egypt Kasr El Ainiy Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Kasr El Aini Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary amount of intraoperative blood loss number of soaked towels during cesarean section
Primary postpartum hemorrhage blood loss after cesarean section 24 hour after cesarean section
Secondary fetal condition apgar score 5 minutes after cesarean section
See also
  Status Clinical Trial Phase
Recruiting NCT03009994 - Exteriorization Versus Non-exteriorization of the Uterus During Repair of Uterine Incision in a Repeated Cesarean Section Phase 2
Completed NCT05664659 - Efficacy of Carbetocin Versus Oxytocin Plus Misoprostol in Decreasing Blood Loss During Cesarean Section Phase 4
Completed NCT03793153 - A Novel Technique Of Uterine Cooling During Repeated Cesarean Section For Reducing Blood Loss N/A