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Evaluation of the surgical result of urethroplasty by vaginal wall flap in female urethral stricture in a pilot study

Evaluation of the surgical result of urethroplasty by vaginal wall flap in female urethral stricture in a pilot study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130306012728N5
Enrollment
10
Registered
2018-06-02
Start date
2017-03-21
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

female urethral stricture. Other urethral stricture

Interventions

Intervention group: Patients with urinary tract stenosis aged over 18 years who indicated stenosis treatment of the urinary tract and had no proper reaction to coservative, drug and dilatation thera

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with urinary tract stricture aged over 18 years who had stricure of the urethra and did not respond to conservative, drug and dilatation treatments, or did not have an informed consent to the above measures, and had a higher than 100 cc pvr , if satisfied with orthoplasty Using the vaginal flap

Exclusion criteria

Exclusion criteria: Patients with skin problems such as Lichen planus or Immunosupercise, or virginal patients, not the deliberate consent of the above surgery [after the describtion], or those who have had neurogenic bladder in the eurorodynamics , are excluded from the action list.

Design outcomes

Primary

MeasureTime frame
Females urethral stricture. Timepoint: 3 to 12 months after intervention. Method of measurement: Eurodynamic- questionnaire.

Secondary

MeasureTime frame
Normal voiding. Timepoint: 3-12 months after intervention. Method of measurement: questionnaire.;Recurrence of symptoms. Timepoint: 3-12 months after intervention. Method of measurement: questionnaire.;Create fistulas. Timepoint: 3-12 months after intervention. Method of measurement: questionnaire and cystoscopy.;Create Incontinence. Timepoint: 3-12 months after intervention. Method of measurement: questionnaire.;Recurrence of stricture. Timepoint: 3-12 months after intervention. Method of measurement: With Eurodynamics and Cystoscopy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Hamed Marofi

Tabriz University of Medical Sciences

hamedmarofi5@gmail.com+98 41 3335 7328

Outcome results

None listed

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