Skip to content

Standard Oxytocin Versus High Dose Oxytocin to Control Postpartum Hemorrhage in High Risk Pregnancy During Elective Cesarean Section

Standard Oxytocin Versus High Dose Oxytocin to Control Postpartum Hemorrhage in High Risk Pregnancy During Elective Cesarean Section

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06560099
Enrollment
39
Registered
2024-08-19
Start date
2024-08-25
Completion date
2025-04-25
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Partum Hemorrhage

Brief 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.

Interventions

DRUGOxytocin

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.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* \- Medical disorders ie: Hypertensive diseases with pregnancy - Diabetes Mellitus - Collagen diseases - Coagulopathies - Cardiac diseases - Anemia * History of postpartum hemorrhage * Placental disorders ie: placenta previa * Infertility and ICSI * High Parity * History of Endometriosis * Fetal disorders (IUGR, IUFD, Preterm, Congenital anomalies, oligohydramnios or polyhydramnios, macrosomia) * Preterm labor on uterine relaxants * Twins pregnancy * Patients on antiplatelets and anticoagulants * Uneventful antenatal care

Exclusion criteria

* \- Oxytocin Allergy * Normal uncomplicated pregnancy * Emergency cesarean section * Exhausted uterus due to trial of normal labor * Couvelaire uterus

Design outcomes

Primary

MeasureTime frameDescription
blood lossat the end of the operationmeasure blood in suction, towels and pads

Secondary

MeasureTime frameDescription
haemoglobinimmediate preoperativeby laboratory asessment

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026