Postpartum hemorrhage

Bilateral uterine artery ligation and square sutures versus a novel combined suture for controlling bleeding from the placental bed in placenta previa centralis at cesarean section: a randomized clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201610001803327

Enrollment

100

Registered

2016-10-03

Start date

2016-10-16

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

Pregnancy and Childbirth Postpartum hemorrhage, cesarean section

Interventions

Bilateral uterine artery ligation and square sutures

novel combined suture

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 100 patients with primary Postpartum hemorrhage (PPH) from the placental bed in cases of placenta previa centralis during cesarean section

Exclusion criteria

Exclusion criteria: Patients with placenta accreta at cesarean section diagnosed on clinical basis (difficult removal of the placenta and excessive maternal hemorrhage) were excluded.

Design outcomes

Primary

Measure	Time frame
Efficacy of the procedure (defined as arrest of bleeding with no need for further interventions).	—

Secondary

Measure	Time frame
duration of the procedure and adverse effects.	—

Countries

Egypt

Contacts

Public ContactMohamed Rezk

Lecturer of Obstetrics and Gynecology-Faculty of Medicine-Menoufia University

m_rezk9207@yahoo.com00201006237186

Outcome results

None listed

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