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临床试验/CTRI/2017/06/008942
CTRI/2017/06/008942尚未招募4 期

Evaluation of Ulipristal in medical management of symptomatic uterine leiomyoma -

College of Medicine and JNM Hospital0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. 18 to 50 years of age group
  • 2. A score on the pictorial blood-loss assessment chart (PBAC, in which monthly scores range from 0 to >500, with higher numbers indicating more bleeding) higher than 100 during days 1 to 8 of menstruation.
  • 3. Fibroid-related anemia, defined as a hemoglobin level of 10.0 g per deciliter or lower.
  • 4. Uterine size equivalent to that of a uterus at 16 weeks or less of gestation.
  • 5. Atleast one fibroid that was 3 cm or more in diameter

排除标准

  • 1. Leiomyoma more than 10 cm
  • 2. Associated with Pregnancy.
  • 3. Who do not agree for consent.
  • 4. Contraindication or known allergy to ulipristal

研究者

发起方
College of Medicine and JNM Hospital

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