Pelvic Organ Prolapse Clinical Trial
Official title:
A Randomized Controlled Study on the Anatomical Reduction and Functional Recovery Effects of Two Transvaginal Apical Slings on Pelvic Organ Prolapse
The study is a prospective study at a single institution. Investigators create strict inclusion and exclusion criteria, selecting 124 patients with POP(≥II degree and have symptoms that need operation) . 62 patients in the intervention group accept extraperitoneal high uterosacral ligament suspension. The other 62 patients in the other group accept sacrospinous ligament suspension.
Investigators evaluate all women's operation method, operation time, bleed volume, overactive bladder questionnaire, PFDI-20,ICIQ-SF, I-QoL, PISQ-12, PFIQ-7, UDI-6, pre- and post-operation (at 1 month, 3 months, 6months and 1 year). ;
Status | Clinical Trial | Phase | |
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Active, not recruiting |
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Phase 2 | |
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BOTOX® at the Time of Prolapse Surgery for OAB
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Phase 4 | |
Completed |
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The 3D Reconstruction Research of Pelvic Organ Prolapse Disease
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N/A | |
Recruiting |
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Not yet recruiting |
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N/A | |
Recruiting |
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N/A | |
Completed |
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N/A | |
Terminated |
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N/A | |
Completed |
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N/A | |
Withdrawn |
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Completed |
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Male Sexual Experience and Its Impact on Quality of Life Before and After Their Sexual Partners Undergo Polypropylene Mesh Augmented Pelvic Floor Reconstruction
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N/A | |
Completed |
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N/A |