Comparison Between Cervical Tourniquet and Uterine Artery Ligation Prior to Segmental Resection Approach

ConditionPlacenta Accreta Spectrum

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexFemale

Age18-38

SponsorMinia University

About this trial

The study will compare a modified surgical approach for preserving fertility and minimizing hemorrhage in morbidly adherent placenta during cesarean section with a cervical tourniquet against uterine artery ligation.

Eligibility criteria

Qualifiers

Diagnosed sonographically to have placenta accreta spectrum .

Pregnancy is singleton and fetus is alive.

Elective caesarean section done from 36 gestational weeks

Disqualifiers

Patients requesting hysterectomy

Coexisting uterine pathology such as fibroids or gynaecological malignancies

Patients with bleeding diathesis.

Morbid obesity of BMI >40.

Trial design

Treatments tested in this trial

cervical tourniquet
uterine artery ligation

Treatment groups

82 Participants

are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Minia University

Lead sponsor

Source ClinicalTrials.gov