N35 N99.1 N32.0
Conditions
Interventions
Group 1: Endoscopic or open surgical treatment of anterior urethral stricture or posterior urethral stenosis, including bladder neck stenosis.
A substantial proportion of the questionnaires listed un
Sponsors
Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients aged 18 years or older who are capable of giving informed consent and undergoing endoscopic or open surgical treatment of a urethral stricture or stenosis.
Exclusion criteria
Exclusion criteria: Patients who are not capable of giving informed consent and individuals under 18 years of age.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| (1) Perioperative Morbidity: Assessment of postoperative complications according to the Clavien-Dindo classification. (2) Patient-Reported Outcome Measures (PROMs): Assessment of validated patient-reported outcomes using the following instruments: - Brief Illness Perception Questionnaire (B-IPQ) - Urethral Stricture Surgery Patient-Reported Outcome Measure (USS PROM) - Urethral Stricture Symptom and Impact Measure (USSIM) - International Prostate Symptom Score (IPSS) - International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF) - International Consultation on Incontinence Questionnaire-Satisfaction (ICIQ-S) - Decision Regret Scale - Male Sexual Health Questionnaire (MSHQ) - International Index of Erectile Function (IIEF) - Oral Health Impact Profile (OHIP) - Patient Global Impression of Change (PGI-C) (3) Retreatment-free Survival: Time interval from the date of index surgery to the occurrence of one of the following events: - Retreatment due to recurrence of urethral stricture or stenosis - Death - Censoring at the date of the last follow-up contact | — |
Countries
Germany
Contacts
Public ContactMalte Vetterlein
Universitätsklinikum Hamburg-Eppendorf
Outcome results
None listed