Trials / Not Yet Recruiting
Not Yet RecruitingNCT06560099
Standard Oxytocin Versus High Dose Oxytocin to Control Postpartum Hemorrhage in High Risk Pregnancy During Elective Cesarean Section
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 39 (estimated)
- Sponsor
- Ain Shams University · Academic / Other
- Sex
- Female
- Age
- 20 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
Controlling hemorrhage during and after a cesarean section reduces significantly maternal mortality and morbidity and the present study is important for detection of the effectiveness of routinely increasing the oxytocin dose instead of using the standard dose only in preventing postpartum hemorrhage and additional use of uterotonics in the first 24 hours after cesarean section for high risk pregnancy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Oxytocin | will receive 10 IU oxytocin intravenous bolus over one min and infusion of 10 IU oxytocin in 500 ml of 0.9 saline over four hours. |
Timeline
- Start date
- 2024-08-25
- Primary completion
- 2025-04-25
- Completion
- 2025-04-25
- First posted
- 2024-08-19
- Last updated
- 2024-08-19
Source: ClinicalTrials.gov record NCT06560099. Inclusion in this directory is not an endorsement.