Autotaxin (ATX) as a Marker for Breast Cancer

NCT04328194 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2020-03-31

No results posted yet for this study

Summary

Breast cancer is the leading cause of cancer death in women worldwide. According to the GLOBOCAN 2018 worldwide estimates of cancer incidence and mortality, in 2018, about 2,088,849 new cases were diagnosed and approximately 626,679 women were predicted to die from the disease . It is the leading cause of cancer related mortality, representing15% of deaths per year worldwide .

Conditions

Interventions

DIAGNOSTIC_TEST

Serum Autotaxin

Marker

RADIATION

chest x-ray

chest x- ray will be done for the study group

DIAGNOSTIC_TEST

Breast ultrasound or mammography

Breast ultrasound or mammography will be done for the study group to diagnosis of breast cancer

DIAGNOSTIC_TEST

Histopathological examination of breast mass specimens

by True cut or fine needle aspiration cytology

RADIATION

Magnetic Resonance Imaging ( MRI) and Bone scan

will be done for the study group

DIAGNOSTIC_TEST

Peripheral haemogram

blood sample will be taken from the patients

DIAGNOSTIC_TEST

Renal and liver functions

to exclude any other morbidity

DIAGNOSTIC_TEST

Prothrombin time and concentration

blood sample will be taken from the patients

DIAGNOSTIC_TEST

Cancer Antigen 15-3 (CA15-3).

will be done for the 2 groups

OTHER

Full medical history

full medical history will be taken from all patients

OTHER

Full clinical examination

full clinical examination will be done for the patients

Sponsors & Collaborators

  • Assiut University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
69 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-05-01
Primary Completion
2022-05-01
Completion
2022-11-01

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04328194 on ClinicalTrials.gov