A Study To Compare Different Treatment Options Available For Short Segment Urethral Strictures in a tertiary care hospital
Not Applicable
Completed
- Conditions
- Health Condition 1: N359- Urethral stricture, unspecified
- Registration Number
- CTRI/2022/05/042436
- Lead Sponsor
- Dr Manjunath Wali
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
Age more than 18years
Patients with Bulbar Urethral Strictures of less than 2cm length
Male patients
Exclusion Criteria
Age less than 18 years
Previous history of urethral surgery (except urethral dilatation and direct Vision Internal Urethrotomy)
Traumatic stricture urethra
Active urinary tract infection
Malignant stricture disease
Patient refusal to participate in the study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Subjective <br/ ><br>1. Urethral Stricture Surgery - Patient Reported Outcome Measure (USS - PROM) scores improvement <br/ ><br>2. Patient Reported Experience Measures (PREM) score improvement <br/ ><br> <br/ ><br>Objective <br/ ><br>1. Qmax in uroflowmetry improvementTimepoint: Immediately after the surgery (post operative day 1) <br/ ><br>1 month, 3months and 6 months after surgery.
- Secondary Outcome Measures
Name Time Method intraoperative parameters including duration of surgery, ease of surhery, amount of blood lost, caliber of diseased urethra, length of stricture and length of harvested mucosal or skin tissue.Timepoint: During the surgery (intraoperative period), <br/ ><br>Post operative day 1, 1 month, 3 months and 6 months after surgery.