Urethral Stricture Database
ConditionUrethral Stricture
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18+
SponsorMedical University of Graz
About this trial
Establishment of a clinical urethral stricture database for a prospective longitudinal cohort study.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Internal urethrotomy according to Sachse (endoscopic transurethral urethrotomy)
End-to-end anastomosis
Urethral plastic surgeries with oral mucosa graft (potentially penile skin)
Urethral plastic surgeries with mesh graft
Disqualifiers
Lack of capacity to consent
Trial population
Patients undergoing urethral surgeries or interventions. All patients meeting the inclusion and exclusion criteria of the study should be informed about the possibility of participating in the study.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Questionnaires and data collection
Other interventionIt is a non-interventional, single-center, non-randomized, prospective observational study obtaining data and patient-reported outcomes.
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Success rate of urethral reconstructive surgeries
Success is defined as a lack of stricture recurrence in the follow-up
Time frame
Questionnaires to patients are captured 3, 6 an d12 months following surgery, and then every year put to 10 yearsSecondary outcomes
1
Complications of urethral reconstructive surgeries
Complications are defined as surgical site infection, fistula, problems at the preservation site of buccal mucosa.
Time frame
Questionnaires to patients are captured 3, 6 an d12 months following surgery, and then every year put to 10 years2
Sexual function after urethral reconstructive surgeries
Time frame
Questionnaires to patients are captured 3, 6 an d12 months following surgery, and then every year put to 10 years3
Health status after urethral reconstructive surgeries
Time frame
Questionnaires to patients are captured 3, 6 an d12 months following surgery, and then every year put to 10 yearsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov