Surgical Classification of Abnormal Placentation

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02736058

Enrollment

100

Registered

2016-04-13

Start date

2016-02-29

Completion date

2016-12-31

Last updated

2016-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adherent Placenta

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.

Interventions

DEVICETrans- abdominal sonography

DEVICETrans-vaginal sonography

PROCEDUREpost-operative pathological specimen examination

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to 45 Years

Healthy volunteers

Yes

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)

Design outcomes

Primary

Measure	Time frame
intraoperative blood loss	24 hours

Countries

Egypt

Contacts

Primary ContactAhmed M Hussein, MD

ahmed_mhussein@live.com01223515652

Backup ContactDina M Dakhly, MD

dinadakhly@gmail.com01003498919

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026