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Evaluation and comparison of the effectiveness of two methods of tension free surgical intervertebral medial autologous sling and synthetic vaginal sling in the correction of stress urinary incontinence

Not Applicable
Conditions
rinary stress incontinence.
Stress incontinence (female) (male)
N39.3
Registration Number
IRCT20211123053163N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
48
Inclusion Criteria

stress urinary incontinence

Exclusion Criteria

Urinary tract infection during surgery
Suspicion of urogenital malignancy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The level of patient satisfaction in urinary control. Timepoint: 3 consecutive months after surgery. Method of measurement: Examination with a cough test and the number of pads used daily.
Secondary Outcome Measures
NameTimeMethod
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