Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
34 participants
INTERVENTIONAL
2021-12-01
2022-06-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact of Netrin-1 in the Pathophysiology of Placenta Accreta Spectrum
NCT04628169
Management of Placenta Accreta Spectrum
NCT04609527
3D Placental Volume in Placenta Accreta
NCT06755047
Creatine Kinase Versus 3D Doppler for Antenatal Diagnosis of Abnormal Adherent Placenta.
NCT03224780
Placenta Accreta Index Score in Placenta Accreta Spectrum
NCT05513092
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Normal pregnancy group
Pregnant women at 28-32 weeks
Pregnant women at gestational age 28-32 weeks
at delivery
women delivered at term
Placenta accreta group
Pregnant women at 28-32 weeks
Pregnant women at gestational age 28-32 weeks
at delivery
women delivered at term
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pregnant women at 28-32 weeks
Pregnant women at gestational age 28-32 weeks
at delivery
women delivered at term
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Singleton pregnancy.
* Women with suspicion of PA by two-dimensional (2D) gray scale imaging and color Doppler flow mapping
Exclusion Criteria
* Fetal anomalies,
* Preterm premature rupture of membranes, or infection
* Any medical disorders, such as thyroid dysfunction, hypertension, and gestational diabetes
* Patients with known bleeding disorders or on anticoagulant therapy.
20 Years
40 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assiut University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohammed Khairy Ali
Assistant professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Woman's Health Hospital
Asyut, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PA-NT1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.