Algazeerah
Giza, Egypt
NCT Number: NCT03416296
Placenta accreta occurs when the placental implantation is abnormal. The marked rise in incidence has been assumed the increasing prevalence of cesarean delivery in recent years.
Looking for future studies?
Notify Me20 year–43 year
Female
Observational
Giza, Egypt
The most accepted theory is that abnormal placentation . The most important risk factor for placenta accreta is placenta previa after a prior cesarean delivery. The first clinical manifestation of placenta accreta is usually severe , life-threatening hemorrhage. The recommended intervention of suspected placenta accreta is planned preterm cesarean hysterectomy with the placenta left in situ.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: within 6 weeks
Aljazeera Hospital
Other
Evaluation of Role of Ultrasound TA,TV,TP in Diagnosis of Placenta Previa and MAP(Morbidly Adherent Placenta )
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03976453
Female Urogenital Diseases and Pregnancy Complications, Morbidly Adherent Placenta
Cairo, Egypt
View Trial DetailsNCT07662187
Conservative Management, Female Urogenital Diseases and Pregnancy Complications
Sohag, Egypt
View Trial DetailsNCT06849349
Female Urogenital Diseases and Pregnancy Complications, Obstetric Labor Complications
Manisa, Turkey (Türkiye)
View Trial DetailsNCT07129135
Abnormal Placentation, Bladder Injury
Cairo, Cairo Governorate, Egypt
View Trial Details