跳至主要内容
临床试验/IRCT20220201053908N1
IRCT20220201053908N1招募中3 期

Comparing the effects of Berberine, Curcumine and gonadotropin-releasing hormone agonist (GnRH) on uterine leiomyoma volume , a controlled, randomized clinical trials

Semnan University of Medical Sciences0 个研究点目标入组 102 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
102

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

年龄范围
18 years 至 45 years(—)
性别
Female

入选标准

  • Non-menopausal women between the ages of 18 and 45, who have a myoma larger than 5 cm that have abnormal uterine bleeding, pelvic pain, dysmenorrhea, and a compressive effect.
  • Women with myomas larger than or equal to 5 cm who have other myomas (s) less than 2 cm in size

排除标准

  • Women with extra myoma (s) greater than or equal to 2 cm
  • Women with uterine myoma who have been treated with any type of estrogen or progesterone in less than a month and hormonal implants in the last 3 months
  • Women with a history of major medical illness and / or previous drug or surgical treatment of uterine leiomyomas
  • All women with myomas 2-5 cm in size were excluded from the study
  • Patients receiving antihypertensive drugs, beta-blockers and calcium channel blockers, and ACE inhibitors were excluded from the study due to possible drug interactions
  • Patients who develop side effects during the study will be excluded from the study

研究者

发起方
Semnan University of Medical Sciences

相似试验