Actively Recruiting
3D Ultrasound Placental Volume and Vascular Indices Versus 2D Parameters for Diagnosis of Placenta Accreta Spectrum
Led by Assiut University · Updated on 2025-01-01
38
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Placenta accreta spectrum disorders (PASD) include abnormal implantation of the placenta into the uterine wall, such as placenta accreta, increta, and percreta. This condition is a significant obstetric concern, and current antenatal diagnostic methods do not provide complete certainty in diagnosis. This study aims to compare two common ultrasound methods, 3D ultrasound and 2D ultrasound with color Doppler, to assess their effectiveness in diagnosing placenta accreta spectrum. The study evaluates 3D ultrasound using placental volume measurements and vascular indices including vascularization index, flow index, and vascularization flow index. The 2D ultrasound assessment includes examining placental invasion criteria such as lacunar vascular flow, abnormal utero-placental interface, myometrial thinning, absence of retroplacental myometrium, interruptions at the utero-vesical interface, and lower uterine segment hypervascularity. These two diagnostic approaches are observed and compared during the study period. Participants will be pregnant women diagnosed with placenta previa and will undergo ultrasound examinations using both 3D and 2D methods. The primary outcome measure is the vascular index assessed at 1 month. Secondary outcomes include evaluation of 2D ultrasound parameters at the same time point. This observational study involves ultrasound imaging to monitor placental characteristics and blood flow, aiming to improve antenatal diagnosis of placenta accreta spectrum disorders.
CONDITIONS
Brief Title
3D Placental Volume in Placenta Accreta
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women with placenta previa
You will not qualify if you...
- Congenital anomalies of the placenta
- Placental separation
- Uterine anomalies
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 month
Participants undergo 3D and 2D ultrasound examinations to assess placental volume and vascular indices for diagnosis of placenta accreta spectrum.
1 to 2 ultrasound visits
Duration - Up to delivery
Participants are monitored for pregnancy outcomes related to placenta accreta spectrum after diagnostic assessments.
Visits according to routine prenatal care
Trial Site Locations
Total: 1 location
1
Women's Health Hospital
Asyut, Egypt
Actively Recruiting
Research Team
M
Mohamed Fekry, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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