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Evaluation of combined electro cutter urethrotomy in the intractable anterior urethral stricture

comparison of combined electro cutter with cold knife with cold knife in the intractable anterior urethral stricture urethrotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201501071981N5
Enrollment
87
Registered
2015-01-15
Start date
2010-05-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

urethral stricture. Postprocedural urethral stricture

Interventions

Intervention 1: in Intervention group :urethrotomy performed by an optical combined electrocutter-cold knife urethrotom internaly in one stage. Intervention 2: in control group:urethrotomy performed b
Treatment - Surgery
in Intervention group :urethrotomy performed by an optical combined electrocutter-cold knife urethrotom internaly in one stage
in control group:urethrotomy performed by a cold knife urethrotom internaly in one stage

Sponsors

Physiology Research Center , Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria :anterior urethral stricture;short and single urethral stricture;recurent urethral stricture exclusion criteria :posterior urethral stricture;long and multiple anterior urethral stricture;first time urethral stricture

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Urethral stricture improve. Timepoint: 15day ,30 day , and 3 months after intervention. Method of measurement: uroflowmetry.;Urethral stricture recurent rate. Timepoint: 15day ,30 day, and 3 months after intervention. Method of measurement: uroflowmetry and retrograde urethrography.

Secondary

MeasureTime frame
Dysuria. Timepoint: 15day ,30 day , and 3 months after intervention. Method of measurement: questionnaire.;Quality of life. Timepoint: 15day ,30 day , and 3 months after intervention. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ali Asghar Ketabchi

Kerman University of Medical Sciences

a_ketabchi@kmu.ac.ir+98 34 3211 4348

Outcome results

None listed

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