Surgical Classification of Abnormal Placentation
Not Applicable
- Conditions
- Adherent Placenta
- Interventions
- Device: Trans- abdominal sonographyDevice: Trans-vaginal sonographyProcedure: post-operative pathological specimen examination
- Registration Number
- NCT02736058
- Lead Sponsor
- Cairo University
- Brief Summary
Reaching the proper pre-operative diagnosis for abnormal placentation in crucial to markedly decrease the intra-operative complications as well as the maternal morbidity and mortality. In this trial researchers aim to set up some pre-operative sonographic criteria that would help in planning the surgical procedure as well as setting up a surgical classification for the abnormally adherent placenta.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
- abnormal placental site (placenta previa)
Exclusion Criteria
- refusal to participate in the study
- cases with normal placental location ( fundal, anterior or posterior wall not reaching the lower uterine segment)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Participants Trans-vaginal sonography the included pregnant females will undergo trans-abdominal sonography as well as trans-vaginal sonography , to diagnose the abnormal placentation and the results will be compared to the intra- operative as well as the pathological examination of the specimen. Participants post-operative pathological specimen examination the included pregnant females will undergo trans-abdominal sonography as well as trans-vaginal sonography , to diagnose the abnormal placentation and the results will be compared to the intra- operative as well as the pathological examination of the specimen. Participants Trans- abdominal sonography the included pregnant females will undergo trans-abdominal sonography as well as trans-vaginal sonography , to diagnose the abnormal placentation and the results will be compared to the intra- operative as well as the pathological examination of the specimen.
- Primary Outcome Measures
Name Time Method intraoperative blood loss 24 hours
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Kasr el aini hospital
🇪🇬Cairo, Egypt