Netrin-1 and Placenta Accreta

NCT ID: NCT04683562

Last Updated: 2022-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-12-01

Study Completion Date

2022-06-01

Brief Summary

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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.

Detailed Description

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Conditions

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Placenta Accreta

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Normal pregnancy group

Group Type OTHER

Pregnant women at 28-32 weeks

Intervention Type OTHER

Pregnant women at gestational age 28-32 weeks

at delivery

Intervention Type OTHER

women delivered at term

Placenta accreta group

Group Type OTHER

Pregnant women at 28-32 weeks

Intervention Type OTHER

Pregnant women at gestational age 28-32 weeks

at delivery

Intervention Type OTHER

women delivered at term

Interventions

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Pregnant women at 28-32 weeks

Pregnant women at gestational age 28-32 weeks

Intervention Type OTHER

at delivery

women delivered at term

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Mohammed Khairy Ali

Assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Woman's Health Hospital

Asyut, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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PA-NT1

Identifier Type: -

Identifier Source: org_study_id

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