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临床试验/NCT01738724
NCT01738724终止4 期

Abnormal Uterine Bleeding in Women With Uterine Leiomyomas: Open Randomized Clinical Trial Of Non Inferiority Between Oral Dienogest, Oral Desogestrel and Subcutaneous Goserelin

University of Sao Paulo0 个研究点目标入组 14 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
14
主要终点
Leiomyoma Volume

研究概览

简要总结

The investigators´aim is to assess whether the progestagen dienogest reduces leiomyoma volume and its associated symptoms to the same extent as gonadotropin releasing hormone (GnRH) analogs or the progestagen desogestrel or whether it is inferior to other drugs already in use.

详细描述

Uterine leiomyoma is a very prevalent condition among women and, although it is mainly asymptomatic, it may be related to bothersome or debilitating symptoms, such as uterine bleeding and pelvic pain or pressure. The standard treatment is surgical (hysterectomy or myomectomy), but there has been continued interest on medical treatments. Progestagens have long been used to control bleeding associated to leiomyomas, but they have not been able to decrease myoma volume. GnRH analogs are well stablished agents, capable of controlling symptoms and decreasing the tumors´volume, but their use is limited by bone loss and menopausal symptoms. A newly introduced progestagen, dienogest, has been studied to treat endometriosis, but its effects on leiomyoma are only starting to be assessed. The investigators are aiming to compare dienogest with the GnRH analog goserelin and the progestagen desogestrel in a randomized trial to see how this new treatment compares with previously used drugs and whether it is similar, inferior or superior to them on controlling leiomyoma associated symptoms and decreasing leiomyoma volume.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
35 Years 至 55 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women with 35 - 55 years of age
  • Uterine volume between 50cc and 500cc
  • Abnormal uterine bleeding probably associated to intramural uterine leiomyomas

排除标准

  • Pregnancy
  • Liver or kidney dysfunction
  • Women with only submucosal or subserosal uterine leiomyomas
  • Women with contraindications to any of the drugs (categories 3 and 4 of WHO eligibility criteria)
  • Use of anticoagulants
  • Others causes of abnormal uterine bleeding (endometrial pathology, cervical pathology)

研究组 & 干预措施

Dienogest

Experimental

Dienogest 2mg pills daily during 6 months

干预措施: Dienogest (Drug)

Goserelin

Experimental

Goserelin 10.8mg preloaded syringe subcutaneously at the start of the study and after 3 months

干预措施: Goserelin (Drug)

Desogestrel

Active Comparator

Desogestrel 75mcg pills daily during six months

干预措施: Desogestrel (Drug)

结局指标

主要结局

Leiomyoma Volume

时间窗: After 6 months of medical therapy

次要结局

  • Pictorial Blood Assessment Chart (PBAC) Score Reduction(After 6 months of medical therapy)
  • Number of episodes of vaginal bleeding(After 6 months of medical therapy)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

LUIZ GUSTAVO OLIVEIRA BRITO

Assistant Physician, MD, PhD

University of Sao Paulo

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