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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03638024
Other study ID # Cell free fetal DNA
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2018
Est. completion date April 3, 2019

Study information

Verified date October 2018
Source Ain Shams Maternity Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cell free fetal DNA might predict abnormal placental invasion


Description:

This study aims to evaluate whether measurement of cell-free fetal DNA in the maternal plasma can be predictive of abnormal invasion in cases of placenta previa.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date April 3, 2019
Est. primary completion date March 3, 2019
Accepts healthy volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion criteria:

1. Maternal age range from 20-40 years old.

2. Parity: para 1- para 5.

3. Body mass index range from 18-25 kg/m2.

4. Singleton pregnancy carrying male fetuses.

5. Gestational age range from 28-34 weeks.

Exclusion criteria:

1. Multifetal pregnancy.

2. Hypertension, preterm labor and intrauterine growth restriction.

3. Patients taking a tocolytic agent or those with uterine bleeding at or after blood sampling.

- Since these complications may increase the level of cell-free fetal DNA.

4. Accidental hemorrhage.

Study Design


Intervention

Diagnostic Test:
Maternal plasma cell free fetal DNA levels
Measurement Maternal plasma cell free fetal DNA levels in both groups (study and control groups)

Locations

Country Name City State
Egypt Ain Shams University, Maternity Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams Maternity Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Predictive value of maternal plasma cell free DNA Prediction of abnormal placental invasion in cases of placenta previa.
Primary aim: Is to evaluate whether measurement of cell-free fetal DNA in the maternal plasma can be predictive of abnormal placental invasion in cases of placenta previa.
Secondary aim: To decrease maternal morbidity and mortality by early prenatal diagnosis of abnormal placental invasion in placenta previa
4 months
Secondary maternal morbidity maternal morbidity 4 months
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