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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ACTIVE_NOT_RECRUITING
80 participants
OBSERVATIONAL
2020-06-01
2026-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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sacrocolpopexy patients
Patients who underwent sacrocolpopexy for the treatment of vaginal cuff prolapse in patients who had previously undergone hysterectomy for benign causes
vaginal cuff prolapse surgery
Different surgical methods for the treatment of vaginal cuff prolapse in patients who have previously undergone hysterectomy for benign causes
lateral suspension surgery patients
Patients who underwent lateral suspension surgery for vaginal cuff prolapse in patients who had previously undergone hysterectomy for benign causes
vaginal cuff prolapse surgery
Different surgical methods for the treatment of vaginal cuff prolapse in patients who have previously undergone hysterectomy for benign causes
Interventions
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vaginal cuff prolapse surgery
Different surgical methods for the treatment of vaginal cuff prolapse in patients who have previously undergone hysterectomy for benign causes
Eligibility Criteria
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Inclusion Criteria
* Patients with symptomatic vaginal cuff prolapse during hysterectomy follow-up
* And for this, patients scheduled for operation
Exclusion Criteria
* Patients with oncology operated for malignant cause
* Non-localized patients with vaginal cuff prolapse
40 Years
75 Years
FEMALE
No
Sponsors
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Kanuni Sultan Suleyman Training and Research Hospital
OTHER
Responsible Party
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Pınar Kadirogulları
Pınar Kadiroğulları M.D, Department of Obstetrics and Gynecology,Principal Investigator
Locations
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Kanuni Sultan Süleyman Training and Research Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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ATADEK- 2020/06
Identifier Type: -
Identifier Source: org_study_id
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