Placenta Accreta Spectrum Topographic Classification
ConditionPlacenta Accreta
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-55
SponsorFundacion Clinica Valle del Lili
About this trial
The present study is a prospective multicenter study consisting of a cohort of patients with prenatal or intraoperative diagnosis of PAS, evaluating the clinical outcomes of the group of patients found in each category of the topographic classification. In addition, an approach to evaluate the acceptability of this classification among the obstetrician-gynecologists of the participating medical centers will be included.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Pregnant woman over 18 years old.
Prenatal diagnosis by ultrasound or MRI of Placenta Accreta Spectrum (PAS), regardless of the suspected degree of severity of the disease.
Case requiring surgical management, either as scheduled or emergent procedure.
Application of the topographic classification of placenta accreta spectrum during laparotomy.
Disqualifiers
None.
Trial population
* Pregnant patients with a diagnosis of placenta accreta spectrum who visits any of the participating medical centers. * Obstetrician-gynecologists working in participating medical centers.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Days of postoperative hospitalization
Number of days the patient was hospitalized from the day of surgery to the day of discharge
Time frame
From the day the surgery is performed until the day of discharge or the date of death from any cause, whichever occurs first, evaluated up to 42 days.2
Volume of intraoperative blood loss
Surgical bleeding calculated in milliliters
Time frame
During surgery3
Bladder injury
Number of patients who had Bladder injuries
Time frame
Up to 42 days postpartum4
Surgical reintervention
Number of patients who need surgical reoperation after index surgery
Time frame
Up to 42 days postpartumSponsors and contacts
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Source ClinicalTrials.gov