temporary uterine artery clamping in cesarean section

The evaluation of the efficiency of temporary uterine artery clamping on postpartum hemorrhage in cesarean section.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201811625172526

Enrollment

200

Registered

2018-11-29

Start date

2018-11-26

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

postpartum hemorrhage

Interventions

Experimental Group

Control Group

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1.Primary singleton cesarean sections 2.BMI<35 kg/m2 3.Between 37-42 weeks pregnancy 4.Between 18-40 ages 5.No any maternal systemic disorders.

Exclusion criteria

Exclusion criteria: 1. Multiple pregnancy 2. Pregnacy plus myoma utery 3. Polyhydramnios 4. Pregnant women with chorioamnionitis 5. Pregnant women with placental abnormalities 6. Pregnant women with bleeding diathesis 7. Pregnant women with low platelet 8. Women who do not want to participate 9. Women who have previous history of postpartum hemorrhage 10. Women with severe adhesion in operation 11.Women with multiparity

Design outcomes

Primary

Measure	Time frame
Preoperative and postoperative hemoglobin, hematocrit and bleeding amount will be measured and recorded. The effects of uterine artery clamping on these variables are examined.	—

Secondary

Measure	Time frame
It will be investigated that the effect of bilateral temporary uterine artery clamping on postpartum hemorrhage in our study.	—

Countries

Somalia

Contacts

Public ContactSafiya Sagal Ahmed

Miss

safiyosagal40@gmail.com+252615937497

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026