Urinary Incontinence Clinical Trial
Official title:
Delivery Method and Risk for Urogenital Prolapse 15-20 Years Later
The lifetime risk for a woman to undergo surgery for either vaginal prolapse or urinary
incontinence is high. Previous studies have shown that pregnancy and childbirth are risk
factors for developing prolapse. There is a lack of studies that follow women several years
after delivery aiming to find whether symptoms of prolapse are linked to delivery method, ie
vacuum, forceps, normal vaginal delivery and cesarean section. The investigators plan this
study is to get more knowledge about pathology of prolapse and incontinence, to enable
development of preventive strategies for these conditions.
Aim of the study is to determine whether the prevalence of symptoms and performed surgery
for urogenital prolapse differs among women delivered by vacuum, forceps, normal vaginal
delivery and cesarean section 15-20 years after their first delivery.
The investigators identify women that delivered their first child at St. Olavs Hospital,
Trondheim, Norway between 1990-1997. Questionnaires will be sent to 2500 women (PFIQ-7,
PFDI-20, PISQ-12), 600 of whom will get a clinical examination, where pelvic floor
musculature is examined by palpation and 4D ultrasound, and a POP-Q quantification of
prolapse performed.
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