Uterine Fibroid Clinical Trial
Official title:
The Effectiveness and Safety of Ulipristal Acetate in Women With Symptomatic Uterine Fibroid
This study evaluates the effectiveness and safety of ulipristal acetae (UPA) in women with symptomatic uterine fibroids. Those who fulfilled inclusion/exclusion criteria will be treated UPA at daily dose of 5mg.
There is increasing evidence approving role of medical therapy in treatment of symptomatic
uterine fibroid, in the context of women's desire to preserve fertility or not to undergo
operation.
Among these hormonal therapies, ulipristal acetate (UPA) is an orally administered selective
progesterone receptor modulator commonly prescribed for treatment of uterine fibroid. This
agent acts on causing apoptosis of the muscle cells inside the tumor and reducing the tumor
matrix in case of uterine fibroid.
UPA at daily dose of 5 mg has been shown to decrease menstrual blood loss and reduce tumor
size after 13 consecutive weeks of treatment.
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