Postpartum Hemorrhage Clinical Trial
Official title:
Efficacy of Oxytocin vs. Carbetocin in Prevention of Postpartum Hemorrhage After Cesarean Section
Verified date | March 2014 |
Source | Shahid Beheshti University of Medical Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Postpartum hemorrhage (PPH) is a common complication of childbirth and a leading cause of maternal morbidity and mortality. The prompt and effective treatment of subjects with PPH would reduce operation risks. Hence in this study, the efficacy of Oxytocin and Carbetocin was compared in prevention of postpartum hemorrhage after cesarean sections.
Status | Completed |
Enrollment | 220 |
Est. completion date | September 2013 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - At least one risk for postpartum hemorrhage and lack of hypersensitivity to oxytocin and carbetocin Exclusion Criteria: - Patients' refusal to cooperate, major therapeutic side effects, history of cardiac and renal disease or preeclampsia |
Country | Name | City | State |
---|---|---|---|
Iran, Islamic Republic of | Infertility and Reproductive Health Research Center | Tehran |
Lead Sponsor | Collaborator |
---|---|
Shahid Beheshti University of Medical Sciences |
Iran, Islamic Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | screening of Cessation of bleeding | screening until 24 hours after placenta disconnection | ||
Primary | time duration to stop bleeding in the case of post-cesarean section | 24 hours |
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