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Effective treatment of vaginal atrophy with isoflavone vaginal gel

Abstract Objetive To assess efficacy and tolerability of a isoflavone ( Glycine max L. Merr.) vaginal gel to the treatment of vaginal atrophy in postmenopausal women. Methods The double-blind, randomized, placebo-controlled, clinical trial. Ninety women were treated for 12 weeks with isoflavone vagi...

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Published in:Maturitas 2013-03, Vol.74 (3), p.252-258
Main Authors: Lima, Sonia M. Rolim Rosa, Yamada, Silvia Saito, Reis, Benedito Fabiano, Postigo, Sostenes, Galvão da Silva, Maria Antonieta L, Aoki, Tsutomu
Format: Article
Language:English
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Summary:Abstract Objetive To assess efficacy and tolerability of a isoflavone ( Glycine max L. Merr.) vaginal gel to the treatment of vaginal atrophy in postmenopausal women. Methods The double-blind, randomized, placebo-controlled, clinical trial. Ninety women were treated for 12 weeks with isoflavone vaginal gel 4% (1 g/day) and a placebo gel and conjugated equine estrogen cream (0.3 mg/day). After 4 and 12 weeks, the vaginal atrophy symptoms were classified at none, mild, moderate and severe and the vaginal cytology were taken to determine the maturation value. The endometrial safety (by transvaginal ultrasonography) was evaluated through at screening and the end of the trial. Results Isoflavone vaginal gel appears to be effective for relief of vaginal dryness and dyspareunia symptons and an increase in the intermediate and superficial cells was noted. These results were similar to the effects with use of conjugated equine estrogens and superior to placebo gel. No changes in endometrial thickness, sera FSH and estradiol levels were observed at study endpoint. Conclusion Glycine max (L.) Merr. at 4% vaginal gel on a daily basis in postmenopausal women led to improvements in vaginal atrophy symptoms and a significant increase in cell maturation values. Isoflavones proved good treatment options for relief of vulvovaginal symptoms especially in women who do not wish to use hormonal therapy or have contra-indications for this treatment.
ISSN:0378-5122
1873-4111
DOI:10.1016/j.maturitas.2012.11.012