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Clinical Trial
. 1994 Jun;46(6):343-6.

[Short-term treatment with leuprolide acetate depot before surgical intervention for uterine leiomyomatosis]

[Article in Italian]
Affiliations
  • PMID: 7936386
Clinical Trial

[Short-term treatment with leuprolide acetate depot before surgical intervention for uterine leiomyomatosis]

[Article in Italian]
R D'Anna et al. Minerva Ginecol. 1994 Jun.

Abstract

It has been amply demonstrated that uterine leiomyoma possess estrogen receptors. On the basis of this presupposition, it is considered logical to use GnRH-agonists which, by reducing the level of estrogen, also reduce the volume of the leiomyoma, although to a varying extent. The maximum reduction which can be obtained occurs, according to published data, between 3 and 6 months of treatment, attaining mean values of approximately 50%. In the author's experience the treatment period was shortened even further by administering only 2 vials of leuprolide depot each month to women who subsequently underwent hysterectomy. The sample group comprised 30 women with uterine leiomyomatosis, of whom 15 were treated with a GnRH analogue and 15 with placebo. The reduction of uterine volume was evaluated by echography and was found to be 40% in the treated group, whereas non change was detected in the "placebo-group".

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