Risk Factors for Recurrence After Pelvic Reconstruction

Status Completed

Clinical Trial Summary

232 women underwent transvaginal mesh repair (TVM)with /without transvaginal hysterectomy for symptomatic POP, including group A（accepted herniamesh polypropylene mesh， 117 patients)；group B （underwent biological graft of cook，115 patients)；follow-ups for six months and one year after the surgery and a questionnaire about the life habits associated with relapse.

Clinical Trial Description

We prospectively study a total of 232 women who underwent transvaginal mesh repair (TVM)with /without transvaginal hysterectomy for symptomatic POP, the patients into two groups :group A was accepted herniamesh polypropylene mesh(117)；group B underwent biological graft of cook(115)；Each patient underwent an interview that included a POP-Q which was quantified according to the Pelvic Organ Prolapse Quantitation (POPQ) system;follow-ups for six months and one year after the surgery and a questionnaire about the life habits associated with relapse. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03457883
Study type	Interventional
Source	Nanjing Medical University
Contact
Status	Completed
Phase	N/A
Start date	January 2015
Completion date	December 2017

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See also
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