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

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Placenta Accreta Spectrum

Treatments

Other: placebo
Drug: oxytocin

Study type

Interventional

Funder types

Other

Identifiers

NCT06493968
Uterotonics in PASD

Details and patient eligibility

About

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

Enrollment

70 estimated patients

Sex

Female

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

70 participants in 2 patient groups, including a placebo group

Group (A)
Experimental group
Description:
Patients will be given uterotonics
Treatment:
Drug: oxytocin
Group (B)
Placebo Comparator group
Description:
Patients will not be given uterotonics
Treatment:
Other: placebo

Trial contacts and locations

1

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Central trial contact

Abdalla Mousa

Data sourced from clinicaltrials.gov

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