Medium-term clinical outcomes following surgical repair for vaginal prolapse with tension-free mesh and vaginal support device |
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| Authors: | T.?Sayer,J.?Lim mailto:jeanettelim@hotmail.com" title=" jeanettelim@hotmail.com" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,J.?M.?Gauld,P.?Hinoul,P.?Jones,N.?Franco,D.?Van?Drie,M.?Slack,for the Prosima Study Investigators |
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| Affiliation: | (1) North Hampshire Hospital, Basingstoke, UK;(2) Royal Women’s Hospital, Melbourne, Australia;(3) Clinical Development, Ethicon, Livingston, UK;(4) Medical Affairs, Ethicon, Somerville, New Jersey, USA;(5) Specialists in Urology, Naples, FL, USA;(6) Women’s Health Center of West Michigan, Grand Rapids, MI, USA;(7) Addenbrooke’s Hospital, Cambridge, UK; |
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| Abstract: | ![]()
Introduction and hypothesis This study was designed to evaluate clinical outcomes ≥2 years following surgery with polypropylene mesh and vaginal support device (VSD) in women with vaginal prolapse, in a prospective, multi-center setting. |
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