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Single Incision Pelvic Floor Mesh Implants

2014-08-27 04:00:43 | BioPortfolio

Summary

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.

Description

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

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Intra-operative Complications

Intervention

Single Incision Mesh, Single Incision Mesh

Location

Assuta MC
Tel Aviv
Israel
45320

Status

Completed

Source

Western Galilee Hospital-Nahariya

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T04:00:43-0400

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