Pre-operative Assessment by Sonourethrography Only in Anterior Urethral Strictures. (PASTIS)
Primary Purpose
Anterior Urethral Stricture, Male
Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Sonourethrography
Sponsored by
About this trial
This is an interventional diagnostic trial for Anterior Urethral Stricture, Male
Eligibility Criteria
Inclusion Criteria:
- Age: 18 years or older
- Anterior urethral strictures (except for meatal strictures)
Exclusion Criteria:
- Posterior urethral strictures
- Meatal strictures
- History of hypospadias repair
- History of phalloplasty
Sites / Locations
- Dept. of Urology, Ghent University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Sonourethrography
Arm Description
Ultrasound of the urethra (Sonourethrography - SUG): In this procedure, a Foley catheter is inserted into the top of the urethra and physiological serum is instilled into the urethra while a linear 7.5 MHz ultrasound probe is placed sagitally on the course of the urethra to detect a narrowing of the urethra.
Outcomes
Primary Outcome Measures
Sonourethrography feasibility: proportion of patients in whom the pre-operative surgical treatment planning was accurate
To evaluate the proportion of patients in whom the pre-operative surgical treatment planning was accurate based on sonourethrography only.
Secondary Outcome Measures
Identification of predictors for failure of treatment planning by sonourethrography by regression analysis.
To evaluate which factors are predictive for failure of treatment planning by sonourethrography only.
Full Information
NCT ID
NCT04452890
First Posted
June 12, 2020
Last Updated
December 5, 2022
Sponsor
University Hospital, Ghent
1. Study Identification
Unique Protocol Identification Number
NCT04452890
Brief Title
Pre-operative Assessment by Sonourethrography Only in Anterior Urethral Strictures.
Acronym
PASTIS
Official Title
PASTIS-Trial: Pre-operative Assessment by Sonourethrography Only in Anterior Urethral Strictures: A Prospective Feasibility Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
July 1, 2020 (Actual)
Primary Completion Date
June 30, 2022 (Actual)
Study Completion Date
June 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Ghent
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The choice of the best surgical technique for urethral stricture repair depends on the stricture length. Estimating the length of urethral strictures is therefore of utmost importance.
Different clinical studies have proven that SUG has a higher sensitivity to evaluate the length of urethral strictures compared to RUG or VCUG.
The goal of this study is to assess the feasibility of using SUG as single pre-operative assessment tool in patients with suspicion of anterior urethral strictures. In this way, use of RUG and/or VCUG could be omitted in the pre-operative work-up of patients with anterior urethral strictures, thereby avoiding significant radiation load of patients.
Detailed Description
Urethral stricture disease (USD) is a medical condition in which a narrowing of the urethral lumen occurs due to pathological fibrosis and cicatrix formation of the urethral mucosa and surrounding spongious tissue (spongiofibrosis). Urethral strictures may occur at any location from the bladder neck to the external urethral meatus and are categorized based on their localisation in anterior strictures (including the urethral meatus, penile urethra and bulbar urethra) and posterior strictures (including the prostatic urethra and membranous urethra). USD is a disease of all ages but the prevalence increases with increasing age since the cumulative risk of having had urethral instrumentation equally increases. All processes that cause urethral trauma may provoke USD. The majority of strictures nowadays is idiopathic or caused by iatrogenic trauma of the urethra.
The pathological narrowing of the urethral lumen can lead to a wide variety of symptoms which ask for specific diagnostic investigations, in which imaging of the urethra plays a central role. Retrograde urethrography (RUG) and voiding cystourethrography (VCUG) are considered to be the gold standard diagnostic investigation techniques for diagnosis of USD.
In both techniques, contrast is instilled in the urethra through the urethral meatus and radiographic imaging is used to visualize the urethra. RUG and VCUG offer the possibility to visualize the urethra completely and to evaluate the number, length and location of urethral strictures. On the other hand, these techniques have some crucial disadvantages. First and foremost, the radiation load of the genitopelvic region in often young patients is inevitable in RUG and VCUG. Secondly, it is impossible to evaluate the degree of spongiofibrosis with radiographic imaging.
In 1988, McAnnich, et al. were the first to describe sonourethrography (SUG) for the diagnosis of anterior urethral strictures in males. In this technique, a Foley catheter is inserted in the urethral meatus and a physiological solution is instilled in the urethra while a linear 7,5 MHz ultrasound probe is placed sagitally over the course of the urethra. SUG is not only able to evaluate the length and localization of a US, but it also enables the investigator to evaluate the grade of spongiofibrosis.
Different strudies have shown that SUG has a higher sensitivity for the measurement of urethral stricture length compared to classical radiographic imaging such as RUG or VCUG. Since the choice of the most adequate surgical technique depends on the length of the urethral stricture, correct estimation of the urethral stricture length is of the utmost importance.
The goal of this study is to evaluate the feasibility of the use of sonourethrography as single diagnostic tool in the pre-operative diagnostic work-up of males with suspicion of anterior urethral strictures. In this way, classic radiographic imaging such as RUG and VCUG could be omitted in these patients, saving them from a significant radiation load.
Fifty patients with penile strictures and fifty patients with bulbar strictures will be included in this study. When 50% of patients (25 penile and 25 bulbar strictures) have completed the study, an interim analysis will be conducted. If this analysis shows that RUG or VCUG can be omitted in 80% or more of patients, the study will be stopped.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Urethral Stricture, Male
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single center, prospective feasibility trial
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sonourethrography
Arm Type
Experimental
Arm Description
Ultrasound of the urethra (Sonourethrography - SUG): In this procedure, a Foley catheter is inserted into the top of the urethra and physiological serum is instilled into the urethra while a linear 7.5 MHz ultrasound probe is placed sagitally on the course of the urethra to detect a narrowing of the urethra.
Intervention Type
Diagnostic Test
Intervention Name(s)
Sonourethrography
Intervention Description
Ultrasound of the urethra.
Primary Outcome Measure Information:
Title
Sonourethrography feasibility: proportion of patients in whom the pre-operative surgical treatment planning was accurate
Description
To evaluate the proportion of patients in whom the pre-operative surgical treatment planning was accurate based on sonourethrography only.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Identification of predictors for failure of treatment planning by sonourethrography by regression analysis.
Description
To evaluate which factors are predictive for failure of treatment planning by sonourethrography only.
Time Frame
2 years
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Only biological males with anterior urethral stricture disease will be included in the study.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age: 18 years or older
Anterior urethral strictures (except for meatal strictures)
Exclusion Criteria:
Posterior urethral strictures
Meatal strictures
History of hypospadias repair
History of phalloplasty
Facility Information:
Facility Name
Dept. of Urology, Ghent University Hospital
City
Ghent
ZIP/Postal Code
9000
Country
Belgium
12. IPD Sharing Statement
Learn more about this trial
Pre-operative Assessment by Sonourethrography Only in Anterior Urethral Strictures.
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