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Diagnostic Value of Strain Elastography in Characterization of Solid Breast Lesions.

Diagnostic Value of Strain Elastography in Characterization of Solid Breast Lesions.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07649590
Enrollment
30
Registered
2026-06-16
Start date
2025-01-01
Completion date
2026-06-01
Last updated
2026-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Solid Breast Lesions

Brief summary

Breast lesions are a common concern in clinical practice, requiring accurate diagnostic tools for effective evaluation. Traditional imaging modalities, such as mammography and ultrasound, play critical roles in detecting and characterizing these lesions. However, the emergence of advanced techniques like strain elastography has significantly enhanced our ability to assess the mechanical properties of breast tissues, providing valuable insights beyond standard imaging. Strain elastography is a non-invasive ultrasound-based technique that evaluates tissue stiffness by measuring the degree of deformation in response to applied pressure. This technique capitalizes on the principle that malignant tissues are typically stiffer than benign ones, offering a potential method for differentiating between solid breast lesions. By assessing the elastic properties of breast tissues, strain elastography aids in improving diagnostic accuracy and reducing the need for unnecessary biopsies. The diagnostic value of strain elastography lies in its ability to provide real-time feedback during ultrasound examinations. This immediacy allows clinicians to make informed decisions about further management based on the mechanical characteristics of the lesions. The integration of strain elastography into routine breast imaging protocols can enhance the specificity and sensitivity of lesion characterization, ultimately benefiting patient outcomes.

Interventions

RADIATIONUltrasound

examination by Ultrasound

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 50 Years

Inclusion criteria

* Woman aged 18 years or older. * Having solid breast lesions identified through mammography or ultrasound and who are scheuduled for biopsy

Exclusion criteria

* Patient with proor breast surgeries * patient who had alocalzied systemic diseases that prevents biopsy. * Inflammtory conditions

Design outcomes

Primary

MeasureTime frameDescription
Assessment of the mass harness by elastographyone yearassessmnet of the mass harness by elasography ration E2/E1

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026