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Study identifier: NCT07403786 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Urethral Resistive Index (URI): A New Parameter for Diagnosing Urethral Obstruction

Condition: Urethral Stricture  ·  Sponsor: Ankara City Hospital Bilkent

PhaseN/A
Planned participants60
Who can joinMale, 18 Years to 80 Years
Healthy volunteersYes

About this study

This prospective observational study aims to evaluate the diagnostic accuracy of a new, non-invasive uroflowmetry parameter called the Urethral Resistive Index (URI) for detecting urethral stricture in men. Currently, diagnosing urethral stricture often requires invasive procedures like surgery or pressure-flow studies. This research seeks to develop URI as a practical and painless screening tool that could reduce the need for such invasive interventions. Study Procedures: A total of 60 male participants (30 with suspected urethral stricture and 30 healthy volunteers) will be enrolled. Participants will undergo two standard, non-invasive uroflowmetry (voiding) tests. The first test is a routine natural voiding session. The second test involves a "forced voiding" (Valsalva maneuver) once the participant feels a sufficient urge to urinate again. The URI is then calculated by comparing the flow rates of these two sessions. Goals and Benefits: The primary goal is to determine the optimal "cut-off" value of the URI that accurately identifies a surgically proven urethral stricture. By demonstrating URI's effectiveness, the study aims to expedite the diagnostic process and spare patients from unnecessary invasive tests. The procedure involves minimal risk, primarily temporary discomfort or psychological stress during the voiding tests

This description comes directly from the study's public registry record.

Talk to the study team

Yusuf Gökkurt  ·  +90-506-791-0557  ·  yusufgokkurt@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Ankara Bilkent City HospitalAnkara, Universiteler, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07403786