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临床试验/NCT02954757
NCT02954757Unknown不适用

Therapeutic Efficacy of High-intensity Focused Ultrasound in the Treatment of Uterine Adenomyosis

Queen Mary Hospital, Hong Kong1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2016年8月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
10
试验地点
1
主要终点
Perceived symptoms change after HIFU treatment By using the menstrual pain score

研究概览

简要总结

Uterine adenomyosis is a common uterine benign condition. They can cause abnormal menstrual bleeding, and menstrual pain. Although surgical intervention is the definitive treatment, some women prefer to have their uterus preserved. High-intensity focused ultrasound (HIFU) therapy is receiving increasing interest in the management of uterine adenomyosis by inducing focal thermocoagulation of the fibroids. Results obtained by various research groups have shown that HIFU treatment is safe, effective and is highly acceptable to patients. The main objective of this study is to evaluate the therapeutic efficacy of HIFU in the treatment of uterine adenomyosis.

In this proposed study, 10 patients who have symptomatic uterine adenomyosis who meet the study inclusion criteria will be invited to participate in the study which involves the use of HIFU in the management of the adenomyosis. Background information of the patients such as age, body mass index, hormonal (pre- or postmenopausal) status and the presence of chronic medical disease will be collected. Subjects will also be asked to complete an eight-item section of a Uterine Fibroid Symptom and Quality Of Life Questionnaire (UFS-QOL) and menstrual pain score which evaluate the effect of the adenomyosis on the quality of life of women.

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 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Age >40 years old, with no future childbearing plans
  • Age >30 years old, who has tubal sterilization
  • Significant symptoms related to adenomyosis, intractable to standard medical therapy, or patient considering radiological intervention (uterine fibroid embolization) or surgery.
  • Clinical uterine size less than 20 weeks gestation
  • Localized adenomyotic lesion or adenomyoma identified of less than 10 cm in diameter as judged by contrast MRI, involving only anterior or posterior uterine wall and not both.
  • No laparotomy scars.
  • Women should be able to give consent.

排除标准

  • Other pelvic or uncontrolled systemic diseases
  • Confirmed or suspected pregnancy
  • Patients who are unable to communicate with researchers during the treatment
  • Patients who are contraindicated for MRI examination
  • Patients with thick abdominal wall (>5 cm, as measured by MRI)
  • Presence or history of acute pelvic inflammatory disease or any pelvic malignancy
  • History of lower abdominal surgery, known severe pelvic endometriosis and/ or extensive pelvic adhesion
  • Presence of significant sized fibroids which may interfere with the treatment or affect the outcome measures

结局指标

主要结局

Perceived symptoms change after HIFU treatment By using the menstrual pain score

时间窗: The changes from baseline to post 12-month treatment will be captured

By using the menstrual pain score for pain evaluation at each follow up (i.e. from baseline to post 1- month, post 1-month to post 3-month, post 3-month to post 6-month, post 6-month to post 12-month treatment will be captured).

次要结局

  • Subsequent management after HIFU treatment of uterine adenomyosis(Up to 12 months)
  • Patient satisfaction score after HIFU treatment of uterine adenomyosis(Up to 12 months)
  • Risks and adverse effects of HIFU in the treatment of adenomyosis(Up to 12 months)
  • Efficacy of HIFU in reducing the size of the adenomyotic lesion and the uterus by sonographic measurements.(The changes from baseline to post 12- month treatment will be captured)
  • Discomfort during procedure by using 10-cm visual analogue scale(immediate after the treatment)
  • Perceived symptoms change after HIFU treatment By using the Uterine Fibroid Symptoms Quality Of Life Questionnaire (UFS_QOL)(The changes from baseline to post12-month treatment will be captured)

研究者

发起方
Queen Mary Hospital, Hong Kong
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Vincent YT Cheung

Dr.

Queen Mary Hospital, Hong Kong

研究点 (1)

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