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Objectives: To evaluate whether the use of single incision un-anchored small mesh implants is feasible, safe and effective for women with moderate pelvic organ prolapse.
Design: Patients diagnosed with moderate pelvic organ prolapse were enrolled to undergo a single incision un-anchored mesh operation. Follow-up was 4 to 23 months. The outcome measures for this study were the operative safety and post-operative pain, adverse effects and anatomical as well as functional cure.
Setting: The operations were performed under general anesthesia according with the reported surgical techniques at university and private hospitals.
Eligibility criteria: female patients with moderate pelvic organ prolapse Outcome measures: intra operative safety and surgical complications, post operative complications and objective as well as subjective cure rates
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Single Incision Mesh | Experimental | intervention: single incision mesh implantation |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Single Incision Mesh | Device | Single Incision Mesh is implanted for pelvic floor reconstruction |
|
| Measure | Description | Time Frame |
|---|---|---|
| Operative mesh related complications | 12 Months |
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Inclusion Criteria:
* Patients with Gr 2-3 Pelvic Organ Prolapse
Exclusion Criteria:
*Previous Pelvic irradiation
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| Name | Affiliation | Role |
|---|---|---|
| Menahem Neuman, Prof. | Western Galilee MC Nahariya | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Assuta MC | Tel Aviv | 45320 | Israel |
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