TCTR20200714001尚未招募4 期
Comparing the effect of depo-medroxyprogesterone acetate (DMPA) and bromocriptine in women with symptomatic myoma uteri: a randomized controlled trial
none0 个研究点目标入组 126 人开始时间: 2020年7月14日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 126
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
- 20 Years 至 50 Years（—）
- 性别
- Female
入选标准
- •1.Woman ages between 20-50 years old.
- •2.Myoma uteri confirmed by transvaginal ultrasound
- •3.Pelvic pain or abnormal uterine bleeding
- •4.Waiting for surgery or premenopausal woman
- •5.Woman who can reading and writing
排除标准
- •1.Heavy uterine bleeding that must have emergency treatment
- •2.Transvaginal ultrasound found other disease in pelvic organ such as ovarian cancer
- •3.Woman who take COC in 1 month or DMPA/implant in 3 months ago
- •4.Deny to taked transvaginal ultrasound
- •5.Pregnancy, lactation or fertility desires
- •6.Abnormal liver or kidney function
- •7.Ergot allergy
- •8.Bleeding disorder
- •9.Contraindication to bromocriptine including allergy, uncontrolled hypertension, pregnancy induced hypertension, myocardial infarction and severe psychological diseases.
- •10.Contraindication to DMPA including uncontrolled hypertension, severe cirrhosis or liver tumor, Kidney or vascular complication from DM , venous thrombosis, cerebrovascular or myocardial infarction, breast cancer and undiagnosed abnormal uterine bleeding
研究者
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