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临床试验/NCT04073485
NCT04073485终止不适用

Microwave Ablation for Uterine Fibroids

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2019年9月5日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
6
试验地点
1
主要终点
Assessment of technical success

研究概览

简要总结

This study is aimed to evaluate the clinical safety and effectiveness of Microwave ablation (MWA) in treating patients with uterine fibroid.

详细描述

Percutaneous radiofrequency ablation (RFA) is another form of thermal ablation that has been used for the treatment of uterine fibroids. Although RFA is more invasive when compared to High-Intensity-Focused-Ultrasound (HIFU), the treatment is less limited by the location of the lesions, and the treatment procedure is more time efficient. To further improve the technology of thermal ablation for uterine fibroid, percutaneous microwave ablation (MWA) could be a promising option because it allows increased efficiency of energy transmission and reduction in procedure time, and may allow effective treatment of large lesions.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
30 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Symptomatic fibroids with or without focal adenomyoma
  • Female gender
  • Age between 30 and 50
  • Pre or peri menopausal with FSH less than 40 mIU/ml
  • Negative urine pregnancy test
  • Uterine size less than 22 weeks based on physical exam assessment
  • Dominant intramural fibroid greater than or equal to 3 cm and less than or equal to 10 cm on imaging.
  • Good health other than history of leiomyomas. Chronic medications may be acceptable at the discretion of the research team.
  • Are using abstinence, mechanical (condoms, diaphragms) or sterilization methods of contraception and are willing to continue using them throughout the study.
  • Willing and able to give informed consent.
  • Willing and able to comply with study requirements.
  • Normal menstrual cycle with endometrial pathology excluded

排除标准

  • History of or current thromboembolic event (deep vein thrombosis, pulmonary embolus, stroke)
  • Other pelvic pathology as indicated by history or MR imaging such as endometriosis, ovarian tumor, acute or chronic pelvic inflammatory disease
  • Pregnant or Positive pregnancy test
  • Unexplained vaginal bleeding
  • Untreated severe cervical dysplasia
  • Abnormal adnexal /ovarian mass
  • Intrauterine device
  • Known recent rapid growth of fibroids, defined as a doubling in size in 6 months
  • Known bleeding tendency
  • Contraindication to MRI due to severe claustrophobia or implanted metallic device.

结局指标

主要结局

Assessment of technical success

时间窗: within one hour

Technical success was defined as successful completion of the planned treatment of target lesions

次要结局

  • Assessment of adverse effects and complications(up to 18 months)
  • Assessment of volume change of the fibroids(15 months after treatment)

研究者

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

Simon Yu

Professor

Chinese University of Hong Kong

研究点 (1)

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