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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03431116
Other study ID # PPLIP
Secondary ID
Status Completed
Phase N/A
First received February 7, 2018
Last updated February 7, 2018
Start date October 1, 2016
Est. completion date April 30, 2017

Study information

Verified date February 2018
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Placenta Previa is defined as a placenta implanted in the lower segment of the uterus, presenting ahead of the leading pole of the fetus (over or near the internal os). The prevalence of placenta previa has been estimated to be approximately 0.5% of all pregnancies, and this increase correlates to the elevated cesarean section rate . In Egypt, the prevalence of placenta previa is around 1.3% in Sohag Governorate and 1.5% in Aswan region according to.

Although various studies have tried to address risk factors associated with Placenta Previa development, the etiology of placenta previa still remains obscure. Several risk actors have been identified as strong contributors to placenta previa development. It is also a significant contributor to severe postpartum hemorrhage.Risk factors include; history of previous cesarean section, advanced maternal age, history of previous abortions, high parity and substance abuse during pregnancy (cigarette smoking), placental size (multiple pregnancy), endometrial damage (previous dilatation and curettage), uterine scars and pathology (previous myomectomy or endometritis), placental pathology (marginal cord insertions and succenturiate lobes), previous placental Previa, and curiously.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date April 30, 2017
Est. primary completion date March 30, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

1. Pregnant women between 18-24 weeks.

2. Diagnosed to have low implanted placenta by ultrasound

Exclusion Criteria:

1. Patient refused to follow-up in our setting.

2. Patient refused to perform Trans-vaginal ultrasound in the second trimester of gestation.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
ultrasound
to detect the placental site

Locations

Country Name City State
Egypt Women Health Hospital - Assiut university Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The distance between lower edge of the placenta and internal os by ultrasound (millimeter) 12 weeks
See also
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