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临床试验/NCT06719934
NCT06719934尚未招募1 期

Dienogest Versus Uterine Artery Embolization in Ttt of Adenomyosis -cohort Comparetive Study

Al-Azhar University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
尚未招募
入组人数
100
试验地点
1
主要终点
evaluation use of Dienogest versus uterine arteries embolization in treatment of Adenomyosis-associated symptoms as dysmenorrhea, heavy menstrual bleeding and bulk-related symptoms by questionnaire

研究概览

简要总结

to evaluate use of Dienogest versus uterine arteries embolization in treatment of Adenomyosis-associated symptoms as dysmenorrhea, heavy menstrual bleeding and bulk-related symptoms

详细描述

Type of the study: prospective cohort comparative study. Setting: It will be done at both Obstetrics & Gynecology department and Radiology department, Al-Azhar University Hospital Assiut branch.

Time of the study: Starting from January 2025 till the end of the study Number of cases: 100 cases. According to sample size equation Where; in: n = number of patients, = 1.96 (standard normal deviate value that divides the central 95% of z distribution from 5% in the tails), P = the reported sensitivity (67%, i.e., 0.67), L= absolute precision desired on either side (half width of the confidence interval of the confidence interval) of sensitivity (10% i.e., 0.1).

Inclusion criteria:

  • Age Group: 30-50 years
  • Women with adenomyosis
  • With or without small fibroids
  • Suffering from heavy menstrual bleeding, dysmenorrhea, and/or cycle- independent pain and bulk-related symptoms.

Exclusion criteria:

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
Single (Participant)

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

  • Age Group: 30-50 years
  • Women with adenomyosis
  • With or without small fibroids
  • Suffering from heavy menstrual bleeding, dysmenorrhea, and/or cycle- independent pain and bulk-related symptoms.

排除标准

  • - Presence of a malignancy or pelvic infection.
  • An on-going pregnancy or a desire to conceive in the future.
  • Absolute contraindication for angiography (renal impairment).
  • Chronic debilitating diseases.

研究组 & 干预措施

Dienogest group

Experimental

will take 2 mg oral Dienogest

干预措施: Dienogest 2 mg orally (Drug)

Uterine artery embolization

Experimental

will undergoes uterine artery embolization by local anasthesia

干预措施: UAE (Procedure)

结局指标

主要结局

evaluation use of Dienogest versus uterine arteries embolization in treatment of Adenomyosis-associated symptoms as dysmenorrhea, heavy menstrual bleeding and bulk-related symptoms by questionnaire

时间窗: through study completion ,an average of 1 year

evaluation use of Dienogest versus uterine arteries embolization in improvement of Adenomyosis-associated symptoms as dysmenorrhea, heavy menstrual bleeding and bulk-related symptoms by questionnaire

次要结局

未报告次要终点

研究者

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

Eshraq Arabi

Assuit

Al-Azhar University

研究点 (1)

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