Evaluation of Planned Conservative Surgical Management of Placenta Accreta Spectrum in Women's Health Center, Assiut University Hospital

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorAssiut University

About this trial

In recent years, with the application of an abdominal artery balloon and the improvement of surgical techniques, efforts are made to preserve the uterus for patients PAS. the aim of the study To evaluate conservative surgical management of placenta accreta spectrum in Assiut University hospital regarding maternal and fetal outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pregnant women with history of previous caesarean section.

Age above 18 years.

Gestational age above 28 weeks.

U/S signs suggestive of placenta previa accreta.

Disqualifiers

Gestational age less 28 weeks.

Age less than 18 years.

Patients with known bleeding disorders.

Multiple pregnancy.

Trial population

patients with placenta accrete spectrum secondary to previous cesarean section and Gestational age above 28 weeks

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

150 Participants
are grouped into 1 trial group
Group A: patients with placenta accrete spectrum

Trial outcomes

Primary outcomes

1

amount of blood loss

amount of blood loss during operation according to number of towels and amount of blood in suction pump

Time frame
baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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