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Role of Uterotonics in Reducing Intraoperative Blood Loss in Patients With PASD Undergoing Cesarean Hysterectomy

Role of Uterotonics in Reducing Intraoperative Blood Loss in Patients With Placenta Accrete Spectrum Disorders Undergoing Cesarean Hysterectomy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06493968
Enrollment
70
Registered
2024-07-10
Start date
2024-07-01
Completion date
2024-12-31
Last updated
2024-07-10

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

Conditions

Placenta Accreta Spectrum

Brief summary

Objectives: To evaluate the effect of oxytocin in reducing intraoperative blood loss in patients with PAS disorders planned for cesarean hysterectomy.

Interventions

DRUGoxytocin

Uterotonics will be given in the form of an IV bolus of 10 units of oxytocin immediately with the uterine incision

OTHERplacebo

IV bolus of normal saline immediately with the uterine incision

Sponsors

Cairo University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnancy of singleton living fetus * Previous one or more cesarean sections * Gestational age: \> 32 weeks * The following ultrasound markers such as loss of clear retroplacental translucency, myometrial thinning, abnormal lacunae, irregular bladder wall, utero-vesicalhypervascularity. * Preoperative hemoglobin more than 10 gm/dl * Cases with PAS that will undergoing CS Hysterectomy

Exclusion criteria

* Maternal medical disorders e.g.: coagulation defects, cardiac diseases etc.…. * Any known or reported hypersensitivity to the used medication. * All cases with spontaneous placental separation at laparotomy. * All patients undergoing conservative management of PAS. * All cases which necessitate emergency termination.

Design outcomes

Primary

MeasureTime frameDescription
Intraoperative blood lossduring operationamount of intraoperative blood loss in patients with PAS disorders undergoing cesarean hysterectomy

Secondary

MeasureTime frame
operative timeduring operation

Countries

Egypt

Contacts

Primary ContactAbdalla Mousa
Dr_abdallamousa@yahoo.com+201277664430

Outcome results

None listed

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