Actively Recruiting

Age: 18Years +
FEMALE
NCT07547891

Shear Wave Elastography for Evaluation of Hydronephrosis in Pregnancy

Led by Beni-Suef University · Updated on 2026-04-27

250

Participants Needed

1

Research Sites

51 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Hydronephrosis is common during pregnancy and is often physiological; however, it may also result from true obstruction requiring intervention. Differentiating between physiological and obstructive hydronephrosis remains a clinical challenge using conventional ultrasound. This prospective observational study aims to evaluate the diagnostic accuracy of renal cortical stiffness measured by shear wave elastography (SWE) in differentiating obstructive from physiological hydronephrosis in pregnant women. Participants presenting with hydronephrosis will undergo clinical assessment, laboratory investigations, and ultrasound evaluation including SWE measurements. The diagnostic performance of SWE will be assessed using receiver operating characteristic (ROC) analysis, and optimal cut-off values will be determined. The study aims to provide a safe, non-invasive, and quantitative tool to improve diagnosis and guide management in pregnant patients with hydronephrosis.

CONDITIONS

Official Title

Shear Wave Elastography for Evaluation of Hydronephrosis in Pregnancy

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women at least 12 weeks gestation with loin pain
  • Sonographic evidence of hydronephrosis
  • Age 18 years or older
  • Provided informed consent
Not Eligible

You will not qualify if you...

  • Chronic kidney disease (CKD)
  • Congenital renal anomalies
  • Pre-eclampsia
  • Poor acoustic window
  • Contraindication to examination position

AI-Screening

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Trial Site Locations

Total: 1 location

1

Beni Suef university hospital

Banī Suwayf, Beni Suef Governorate, Egypt, 62511

Actively Recruiting

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Research Team

M

Mahmoud Abdallah Mahmoud, lecturer of urology

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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