ConditionObstetric Complication
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-40
SponsorCairo University
About this trial
Placenta accreta rates are rising alongside the rising rates of caesarean deliveries. This has lead to a vast number of studies negotiating the histopathological nature, risk factors and outcomes of pregnancies complicated with placenta accreta. In the study the investigators re discussing the outcome of different plans of management of placenta accreta, namely caesarean hysterectomy and focal myometrium resection.
Eligibility criteria
Qualifiers
Singleton pregnancy with living fetus
Average liquor: 5-25 cm
Gestational age ≥ 34 weeks at time of termination
Previous lower segment cesarean section/s
Disqualifiers
Hepatic, cardio-pulmonary or coagulation disorders
Hemoglobin< 9.5g/dl
Ruptured membranes
Need for emergency delivery as Antepartum hemorrhage or contractions
Trial design
Treatments tested in this trial
- Caesarean Hysterectomy
- Conservative management
Treatment groups
36 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov