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PATIENT-REPORTED OUTCOME MEASURE FOR URETHRAL STRICTURE SURGERY

Not Applicable
Conditions
Health Condition 1: N51- Disorders of male genital organs in diseases classified elsewhere
Registration Number
CTRI/2020/02/023578
Lead Sponsor
MUMMALANENI SITARAM
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients suffering with bulbar urethral stricture who are undergoing urethroplasty or visual internal urethrotomy and aged between 18 years and 60 years are included.

Exclusion Criteria

patients who had urethroplasty or visual internal urethrotomy prior to study period

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
TO EVALUATE <br/ ><br>1.LUTS <br/ ><br>2.ERECTILE FUNCTION <br/ ><br>3.EJACULATORY FUNCTION <br/ ><br>AS REPORTED BY THE PATIENT USING LUTS,ERECTILE AND EJACULATORY FUNCTION SCORES.Timepoint: 1.PRE-OPERATIVELY <br/ ><br>2.AT 3 MONTHS POST OPERATIVELY <br/ ><br>3.AT 6 MONTHS POST OPERATIVELY <br/ ><br>4.AT 12 MONTHS POST OPERATIVELY
Secondary Outcome Measures
NameTimeMethod
EVALUATE <br/ ><br>1.HEALTH RELATED UALITY OF LIFE AS REPORTED BY PATIENT USING (EQ-5D) QUESTIONNAIRE <br/ ><br>Timepoint: .PRE-OPERATIVELY <br/ ><br>2.AT 3 MONTHS POST OPERATIVELY <br/ ><br>3.AT 6 MONTHS POST OPERATIVELY <br/ ><br>4.AT 12 MONTHS POST OPERATIVELY
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