Prospective study of single incision transvaginal mesh with apical fixation to treatment of anterior vaginal wall prolapses

Not Applicable

• Conditions: anterior vaginal wall prolapse; apical vaginal prolapse; stress urinary incontinence; Surgery - Surgical techniques; Renal and Urogenital - Other renal and urogenital disorders

• Registration Number: ACTRN12610000879066
• Lead Sponsor: Promedon

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2010-10-19
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

female
pregnancies defined
no diseases with contraindications for anesthesia
anterior vaginal prolapse with point Ba > +1 (POP-Q classification)

Exclusion Criteria

point Bp > -1 or point C > -1 (POP-Q classification),
without tumoral diseases
without urinary infections
without vaginal infections
no previous radioterapy
no pregnancy
no blood dyscrasias or immunosuppression
no psychiatric or neurological diseases

Study & Design

• Study Type: Interventional
• Study Design: Not specified