Details

Autor(en) / Beteiligte

• BAGARIA, Madhu
• SUNEJA, Amita
• VAID, Neelam B.
• GULERIA, Kiran
• MISHRA, Kiran

Titel

Low-dose mifepristone in treatment of uterine leiomyoma: A randomised double-blind placebo-controlled clinical trial

Ist Teil von

• Australian & New Zealand journal of obstetrics & gynaecology, 2009-02, Vol.49 (1), p.77-83

Ort / Verlag

Melbourne, Australia: Blackwell Publishing Asia

Erscheinungsjahr

2009

Quelle

Access via Wiley Online Library

Beschreibungen/Notizen

• Aims: To evaluate the effect of low‐dose mifepristone on leiomyoma‐related symptoms, uterine and leiomyoma in women with symptomatic leiomyomata. Methods: In a double‐blind placebo‐controlled trial, 40 patients with symptomatic leiomyoma and normal endometrial histology were randomised to receive 10 mg mifepristone (group 1) or placebo (group 2) daily for three months. Leiomyoma‐related symptoms, uterine, leiomyoma and largest leiomyoma volumes were assessed at baseline and every month for three months. Endometrial biopsy was repeated at the end of therapy. Results: Significant change was noticed between the two groups for mean menstrual blood loss (MBL) by first month. Menstrual blood loss declined by 94.8% in group 1 at three months and 84.2% patients attained amenorrhoea in this group. In group 1 complete relief of dysmenorrhoea occurred in significant number of women (80%) but only 33% patients got rid of pelvic pain. There was no change in these symptoms in group 1 Backache, urinary complaints and dyspareunia were not relieved in either group. Uterine, leiomyoma and largest leiomyoma volume declined by 26–32% in group 1 as compared to none in group 2, and this difference was statistically significant only by the end of the third month of therapy. Mean haemoglobin increased from 9.5  to 11.2 g/dL in group 1. In group 1, at the end of therapy, 63.1% of patients had endometrial hyperplasia without atypia. Conclusions: Ten milligrams mifepristone for three months is effective in reducing MBL, increasing haemoglobin and reducing uterine and leiomyoma volume with side‐effect of endometrial hyperplasia.