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Clinical Trial
. 1992 Dec;15(3):241-9.
doi: 10.1016/0378-5122(92)90208-l.

Preoperative treatment with oestradiol in women scheduled for vaginal operation for genital prolapse. A randomised, double-blind trial

Affiliations
Clinical Trial

Preoperative treatment with oestradiol in women scheduled for vaginal operation for genital prolapse. A randomised, double-blind trial

C Felding et al. Maturitas. 1992 Dec.

Abstract

Objective: To disclose a clinical and histopathological effect of local low-dose oestradiol treatment on the vagina.

Design: A randomised, double-blind trial.

Setting: Two gynaecological departments at University Hospitals.

Subjects: Forty-eight postmenopausal women scheduled for surgery because of genital prolapse.

Intervention: 25 micrograms oestradiol or placebo, administered as vaginal pessaries daily, 3 weeks prior to surgery.

Main outcome measures: Cytological, histological and clinical changes of the vaginal mucosa.

Results: The thickness of the vaginal wall increased as did the oestrogenic index. No clinical effect was seen apart from decreased incidence of recurrent cystitis postoperatively.

Conclusions: Preoperative oestrogen treatment has been shown to reduce the incidence of recurrent cystitis and may be needed for stimulation of vaginal mucosa; the short-term clinical effect is not convincing, however.

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