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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01246271 |
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Date of registration:
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19/11/2010 |
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Primary sponsor: |
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Public title:
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Sub Urethral Sling With or With Out Anterior Repair
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Scientific title:
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a Retrospective Cohort Recognize the Out Comes of SUS With or Without Anterior Vaginal Repair |
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Date of first enrolment:
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February 2008 |
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Target sample size:
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98 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01246271 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Retrospective
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Countries of recruitment
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Iran, Islamic Republic of
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Patients must be female
2. Subjective evidence of stress predominant symptoms on symptom specific questionnaire
3. Stress incontinence on urodynamics
4. Patients must be capable of filling in the symptom diary
5. Prolapse beyond the introitus
Exclusion Criteria:
1. Patients who are medically unfit to undergo surgical intervention.
2. Patients who have undergone previous continence surgery
3. Patients with voiding dysfunction
4. Patients with recurrent urinary tract infection
5. Patients who are not sure that their family is complete
Age minimum:
27 Years
Age maximum:
78 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Urinary Incontinence
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Primary Outcome(s)
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Urinary incontinence cure rate according ICIQ-UIsf
[Time Frame: 3 month after surgery]
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Secondary Outcome(s)
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morbidity and complication
[Time Frame: 3 month after surgery]
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Secondary ID(s)
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89-234
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8948
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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