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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04683562
Other study ID # PA-NT1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2021
Est. completion date June 1, 2022

Study information

Verified date August 2022
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Netrin-1 is a secreted protein, which was first identified as a neuronal guidance factor. It is expressed in a multitude of tissues as pancreas, lung, breast, and placenta. Netrin-1 is a multifunctional protein, involved in cell polarity, adhesion, angiogenesis, apoptosis, migration, morphogenesis, and differentiation of various cell types. Most of netrin-1 activity occur through signaling pathways induced by its two main receptors, DCC (deleted in colorectal cancer) and UNC5H (uncoordinated-5 homolog). Its receptors have been linked to the processes of apoptosis and angiogenesis. In absence of netrin-1, DCC and UNC5H receptors lead to apoptosis. In contrary, in presence of netrin-1, receptors transduce molecular cascades leading to proliferation, differentiation and migration of the cells. Netrin-1 has been involved in the pathogenesis of multiple diseases, as diabetes, cardiovascular diseases, and cancer. Serum Netrin-1 levels were high in preeclamptic patients.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date June 1, 2022
Est. primary completion date June 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - Age between 20-40 years. - Singleton pregnancy. - Women with suspicion of PA by two-dimensional (2D) gray scale imaging and color Doppler flow mapping Exclusion Criteria: - Multiple pregnancy, - Fetal anomalies, - Preterm premature rupture of membranes, or infection - Any medical disorders, such as thyroid dysfunction, hypertension, and gestational diabetes - Patients with known bleeding disorders or on anticoagulant therapy.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pregnant women at 28-32 weeks
Pregnant women at gestational age 28-32 weeks
at delivery
women delivered at term

Locations

Country Name City State
Egypt Woman's Health Hospital Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Placental Netrin-1 level will be measured by using enzyme-linked immunosorbent assay (ELISA) in placental homogenate 4 weeks
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