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

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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • cervical tourniquet

    Procedure/Surgery

    After opening the abdominal wall, To reduce bleeding during PAS, make the uterine incision above the placenta's intrauterine borders . 2-investigators extract the uterus from the abdomen 3-An assistant slides a sterile Foley catheter (Ch 16/18 French) down to the lowest point and secures it "en bloc" around the cervix 4-The bladder peritoneum is isolated from the uterus 5-To remove myometrial tissue, leave a margin of at least 2 cm superior to the cervical internal ostium using electrocautery or scissors .

  • uterine artery ligation

    Procedure/Surgery

    After opening the abdominal wall, To reduce bleeding during PAS, make the uterine incision above the placenta's intrauterine borders . 2-investigators extract the uterus from the abdomen 3-The bladder peritoneum is isolated from the uterus 4-The uterine vessels were ligated in continuity at the level of the utero-vesical fold on each side 5-To remove myometrial tissue, leave a margin of at least 2 cm superior to the cervical internal ostium using electrocautery or scissors .

Treatment groups

82 Participants
are divided into 2 treatment groups
Group A: Group 1 (n = 41) cervical tourniquetExperimental treatment 1 intervention
Group B: Group 2 (n=41) uterine artery ligationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

operation time

recording total time of the surgery

Time frame
intraoperative
2

repair time

recording length of defect repair from placental separation until uterine wall closure

Time frame
intraoperative
3

Estimated blood loss

recording amount of blood loss

Time frame
intraoperative
4

packed red blood cells transfusion

recording amount of red blood cell transfused

Time frame
intraoperative until 24 hours after surgery

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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