Evaluation of the Results of Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh in the Surgical Treatment of Pelvic Organ Prolapse
NCT ID: NCT06176521
Last Updated: 2025-08-06
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
35 participants
INTERVENTIONAL
2023-11-01
2025-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh
Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh
Comparison of pre and postoperative POP-Q values of the patients undergone Laparoscopic Sacrohysteropexy and Sacrocolpopexy SurgeriesWithout Using Mesh Comparison of pre and postoperative PISQ-12 scores of the patients undergone Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Without Using Mesh
Interventions
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Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh
Comparison of pre and postoperative POP-Q values of the patients undergone Laparoscopic Sacrohysteropexy and Sacrocolpopexy SurgeriesWithout Using Mesh Comparison of pre and postoperative PISQ-12 scores of the patients undergone Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Without Using Mesh
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. needing an operation for symptomatic pelvic organ prolapse -
Exclusion Criteria
2. past history of pelvic organ prolapse surgery
3. if there is a contraindication of laparoscopy -
18 Years
FEMALE
No
Sponsors
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Gaziosmanpasa Research and Education Hospital
OTHER_GOV
Responsible Party
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Locations
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Gaziosmanpasa Training and Research Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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GaziosmanpasaTREHs
Identifier Type: -
Identifier Source: org_study_id
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