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Evaluation of Different Surgical Approaches Used for Conservative Management of Placenta Accreta Spectrum in Sohag University Hospital

S

Sohag University

Status

Enrolling

Conditions

Placenta Accreta Spectrum

Study type

Observational

Funder types

Other

Identifiers

NCT05510076
Soh-Med-22-08-03

Details and patient eligibility

About

The objective of this study is to evaluate different intra-operative procedures to control bleeding in cases of PAS disorders aiming to determine the best procedure regarding maternal morbidity and mortality post-operatively, and to evaluate the long-term effects of conservative management of PAS disorders.

Full description

The term "placenta accreta spectrum" (PAS), formerly known as "morbidly adherent placenta" or "abnormally invasive placenta," refers to the aberrant trophoblast invasion of all or a portion of the placenta into the myometrium of the uterus. according to the depth of the villous invasion into the myometrium, the spectrum is assorted into three groups: placenta accreta (villi attach to the myometrium without invading it), placenta increta (villi infiltrate the myometrium), and placenta percreta (villi pierce through the uterine serosa and may infiltrate the surrounding tissues). The optimal strategy for managing PAS disorders remains debatable. Conservative management of PAS disorders includes all techniques aimed at preserving the uterus. Because intraoperative bleeding from PAS disorders is frequently massive and dramatic, causing severe maternal morbidity and mortality, it is essential to have a well-planned, effective, and rapid approach to this surgical challenge.

Enrollment

60 estimated patients

Sex

Female

Ages

Under 51 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women with at least one previous caesarean section and suspected PAS disorders by imaging studies

Exclusion criteria

  • Patients with intraoperative spontaneous placental separation.
  • Patients with a preoperative diagnosis of placenta percreta who chose to have an elective hysterectomy.
  • Any other associated uterine pathology requiring hysterectomy.
  • Coagulation disorders.

Trial design

60 participants in 3 patient groups

Group A
Description:
in which full-thickness vertical compression suture combined with inflated intrauterine balloon are used to control bleeding
Group B
Description:
in this group, a resective-reconstructive technique is used, which involves resecting the invasive accreta area followed by immediate uterine reconstruction and bladder reinforcement
Group C
Description:
In this group, bilateral uterine artery ligations combined with cervical tamponade which is performed by elevating the cervix into the uterine cavity with Allis forceps, then suturing the anterior and/ or posterior cervical lip(s) into the anterior and/ or posterior uterine segment(s) depending on the site of bleeding with two or three simple interrupted stitches, with the patency of the cervical canal confirmed, followed by closure of the uterine incision

Trial contacts and locations

1

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Central trial contact

AbdAllah Refaat; AbdAllah Refaat

Data sourced from clinicaltrials.gov

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