Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2017-04-25
2018-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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cystocele
Arm: Patients with paravaginal defect cystocele
Intervention: transobturator approach for paravaginal repair
transobturator approach for paravaginal repair
using TOT needle to apply suturs to white line
Interventions
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transobturator approach for paravaginal repair
using TOT needle to apply suturs to white line
Eligibility Criteria
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Inclusion Criteria
* midline and paravaginal defect cystocele
Exclusion Criteria
* previous cystocele surgery
20 Years
50 Years
FEMALE
Yes
Sponsors
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Ain Shams Maternity Hospital
OTHER
Responsible Party
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Hamdy Ahmed Saaid
Dr.Hamdy Ahmed
Principal Investigators
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Hazem SH Samoor, Professor
Role: STUDY_CHAIR
Ain Shams Universty
Locations
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Urogynecology Unit
Cairo, , Egypt
Countries
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Other Identifiers
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PVRNA
Identifier Type: -
Identifier Source: org_study_id
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