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Clinical Trial
. 1998 Aug;33(8):490-2.

[A clinical control study on the treatment of uterine leiomyoma with gonadotrophin releasing hormone agonist or mifepristone]

[Article in Chinese]
Affiliations
  • PMID: 10806751
Clinical Trial

[A clinical control study on the treatment of uterine leiomyoma with gonadotrophin releasing hormone agonist or mifepristone]

[Article in Chinese]
C Zeng et al. Zhonghua Fu Chan Ke Za Zhi. 1998 Aug.

Abstract

Objective: To compare the results and side effects in treating uterine leiomyoma with gonadotrophin releasing hormone agonist (GnRH-a) or mifepristone.

Methods: 75 patients with uterine leiomyoma who had clinical symptoms and diagnosed by Bcan were divided into two groups. The GnRH-a group (30 patients) was treated by injection of GnRH-a 150 micrograms/day subcutaneously for three months, and the mifepristone group (45 patients) was treated by mifepristone 12.5 mg/day po for three months.

Results: The clinical symptoms improved obviously in both groups. The volume of leiomyoma reduced 20.0% or more in 90.0% (27/30) of the patients in GnRH-a group, while it was 91.1% (41/45) in mifepristone group. However, the recurrent rates were 40.0% and 17.8% in the 2 groups.

Conclusion: It suggested that mifepristone is a more practical and hopeful drug in treating uterine leiomyoma.

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