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Enrolling by invitation NCT07075666

Early Detection of Prostate Cancer of Syrian Men

Observational the Detection of Prostate Cancer in Men

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: PSA, DRE.
Who it may be relevant to
Registry conditions: the Detection of Prostate Cancer in Men. Basic parameters: 40 years — 65 years · Male.
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 Prostate Cancer Among Men in the Middle Region of Syria

Overview

Prostate cancer is a significant health concern in the Middle East, including Syria, where many cases are diagnosed at advanced stages due to low awareness and inadequate screening practices. The mortality-to-incidence ratio for prostate cancer in the region is alarmingly high, indicating a pressing need for effective early detection strategies.

Detailed description

This study aims to assess the awareness, attitudes, and practices regarding prostate cancer screening among men in the middle region of Syria, with the goal of identifying barriers to early detection and informing public health interventions.

Interventions

  • Diagnostic test PSA
    Prostate-Specific Antigen test, a blood test used to measure the level of PSA in a man's blood. PSA is a protein produced by the prostate gland, and elevated levels can indicate various conditions, including prostate cancer, benign prostatic hyperplasia (BPH), or prostatitis.
  • Diagnostic test DRE
    A digital rectal exam (DRE) is a procedure where a doctor inserts a lubricated, gloved finger into the rectum to check for abnormalities.

Primary outcome measures

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

Eligibility criteria

Inclusion criteria

  • Men aged 40 years and older residing in the middle region of Syria.

Exclusion criteria

  • Men with a previous diagnosis of prostate cancer.

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

Study design

Observational model
Cohort

Study locations

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

Identifiers

NCT: NCT07075666 · 02-05-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗