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Different routes and forms of uterotonics for treatment of retained placenta

Different routes and forms of uterotonics for treatment of retained placenta: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10193593
Enrollment
281
Registered
2014-06-03
Start date
2014-06-08
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Retained placenta Pregnancy and Childbirth Retained placenta without haemorrhage

Interventions

The enrolled participants will be allocated randomly into three groups. The trial allocation sequence for all cases enrolled will be developed using a computer-generated random number table. Sequentia

Sponsors

Al-Hayat National Hospital (Saudi Arabia)
Lead Sponsor
Menoufiya University Hospital (Egypt)
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Booked or un-booked patients who deliver in the study hospitals or those who are transferred to them after delivering elsewhere 2. Gestational age of 28 weeks or more (updated 11/08/2015: was previously 20 weeks or more) 3. Singleton pregnancies 4. =30 minutes interval after the delivery of the baby provided that our routine active management of the third stage was implemented

Exclusion criteria

Exclusion criteria: 1. Maternal hemodynamic instability requiring immediate intervention (pulse > 100 beats per minute, systolic blood pressure <100 mmHg, diastolic blood pressure reduction more than 20 mmHg) 2. Severe postpartum hemorrhage requiring immediate intervention 3. History of RP or MROP in any previous delivery 4. Vaginal birth after previous cesarean scar 5. Associated medical disorders (e.g., pre-eclampsia, gestational hypertension, pre-gestational and gestational diabetes, cardiac diseases) 6. Placenta previa in the current pregnancy or previous pregnancies 7. Stillborn baby 8. Snapped umbilical cord 9. Known uterine anomalies

Design outcomes

Primary

MeasureTime frame
1. Delivery of the placenta within 30 minutes following drug administration (either spontaneously or following controlled cord traction) 2. The need for MROP

Secondary

MeasureTime frame
1. Post-partum hemorrhage defined as drop in the hemoglobin of 2 g/dl between the pre-randomization level or that taken at least 2 weeks before delivery and the hemoglobin measured 24 hours after delivery 2. Need for blood transfusion at any time before discharge from the hospital 3. Need for additional uterotonic agents to control post-partum hemorrhage 4. Need for uterine curettage

Countries

Egypt, Saudi Arabia

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026