Menu
Enrolling by invitation NCT07056686

Early Detection of Breast Cancer Among Syrian Women

Observational Breast Cancer Detection

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Mammogram.
Who it may be relevant to
Registry conditions: Breast Cancer Detection. Basic parameters: 18 years — 65 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Syria
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Early Detection of Breast Cancer Among Women in the Middle Region of Syria

Overview

The goal of this observational study is to evaluate breast cancer awareness, screening practices, and barriers to early detection among women in the middle region of Syria. The main questions it aims to answer are: 1. What is the level of awareness among women in this region regarding breast cancer symptoms and risk factors. 2. How do women practice breast self-examination and professional screenings. 3. What barriers prevent women from seeking early detection and treatment? Participants will complete a survey assessing their knowledge, behaviors, and challenges related to breast cancer screening. The findings will inform public health interventions to improve awareness and early detection practices.

Interventions

  • Diagnostic test Mammogram
    Each patient will undergo a mammogram and echo of the breast used to detect early signs of cancer, such as tumors or calcifications, before symptoms appear.

Primary outcome measures

  • Number of Participants with early signs of breast cancer [Time frame: From Participant enrolment to the end of the study at 2 weeks]

Eligibility criteria

Women aged 18 years and older residing in the middle region of Syria.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Syria · 1 center
  • Al-Hawash Private University — Homs

Identifiers

NCT: NCT07056686 · 01-05-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗