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PATIENT-REPORTED OUTCOME MEASURE FOR URETHRAL STRICTURE SURGERY

A PROSPECTIVE PATIENT-CENTRED EVALUATION OF VISUAL INTERNAL URETHROTOMY AND URETHROPLASTY FOR URETHRAL STRICTURE USING A PATIENT-REPORTED OUTCOME MEASURE

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/02/023578
Enrollment
100
Registered
2020-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N51- Disorders of male genital organs in diseases classified elsewhere

Interventions

Control Intervention1: NIL: NIL

Sponsors

MUMMALANENI SITARAM
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
TO EVALUATE 1.LUTS 2.ERECTILE FUNCTION 3.EJACULATORY FUNCTION AS REPORTED BY THE PATIENT USING LUTS,ERECTILE AND EJACULATORY FUNCTION SCORES.Timepoint: 1.PRE-OPERATIVELY 2.AT 3 MONTHS POST OPERATIVELY 3.AT 6 MONTHS POST OPERATIVELY 4.AT 12 MONTHS POST OPERATIVELY—

Secondary

MeasureTime frame
EVALUATE 1.HEALTH RELATED UALITY OF LIFE AS REPORTED BY PATIENT USING (EQ-5D) QUESTIONNAIRE Timepoint: .PRE-OPERATIVELY 2.AT 3 MONTHS POST OPERATIVELY 3.AT 6 MONTHS POST OPERATIVELY 4.AT 12 MONTHS POST OPERATIVELY—

Countries

India

Contacts

Public ContactMUMMALANENI SITARAM

KASTURBA HOSPIATAL

urologyarun@yahoo.com8121142544

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026