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Surgical Classification of Abnormal Placentation

Not Applicable
Conditions
Adherent Placenta
Interventions
Device: Trans- abdominal sonography
Device: Trans-vaginal sonography
Procedure: 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
GroupInterventionDescription
ParticipantsTrans-vaginal sonographythe 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.
Participantspost-operative pathological specimen examinationthe 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.
ParticipantsTrans- abdominal sonographythe 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
NameTimeMethod
intraoperative blood loss24 hours
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Kasr el aini hospital

🇪🇬

Cairo, Egypt

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