Comparative study of outcomes following two techniques of substitution uretheroplasty
Not Applicable
- Conditions
- Health Condition 1: null- Anterior uretheral strictureHealth Condition 2: N359- Urethral stricture, unspecified
- Registration Number
- CTRI/2018/07/015028
- Lead Sponsor
- Department of Urology PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Inclusion criteria
•Strictures >2cm involving bulbar urethra, >1 cm involving penile urethra
•Patients requiring repeated internal urethrotomy or dilatations.
Exclusion Criteria
Exclusion criteria
•Periurethral phlegmon,
•Multiple urethrocutaneous fistula
• Scarred perineum.
• Severe oral cavity infection
• Mucosal ulceration
• Mucosal fibrosis
• Mucosal white or red patches
• Circumscised or unhealthy/unavailable preputial skin
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional outcomes-post op LUTS(International Prostate Symptom Score (IPSS), post op erectile function(International Index of Erectile Func- tion (IIEF) questionnaires, post op ejaculatory function(MSHQ-EJD questionnaire),post op penile sensation,post op lower urinary tract pain <br/ ><br> <br/ ><br> <br/ ><br>Timepoint: pre operative, in post operative period-at 3 weeks,6 weeks,3 months,6 months,12 months, every 6 months thereafter. <br/ ><br>minimum follow up of 3 months
- Secondary Outcome Measures
Name Time Method Anatomic outcomes-Uroflowmetry,RGU,CystoscopyTimepoint: pre operative, in post operative period-at 3 weeks,6 weeks,3 months,6 months,12 months, every 6 months thereafter. <br/ ><br>minimum follow up of 3 months