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临床试验/IRCT138903013881N2
IRCT138903013881N2已完成未知

Comparison of short-term complications (mensturation patern), satisfaction and quality of life in Mirena users as a contraception method with Copper IUD users

Vice chancellor for research of Tehran University of Medical Sciences0 个研究点目标入组 160 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
160

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 35 years(—)
性别
Female

入选标准

  • age20-35; normal menstruation; multi-parity and a negative pop smear result in the previous six months. Exclusion criteria: pregnancy; abnormal menstruation (irregularity, oligomenorrhea, hypermenorrhea and menorrhagia); malignancies of uterine; ovaries and breasts; a personal and familial history of mass in breasts; uterine anomaly or myoma; pelvic inflammatory disease; psychiatric disorders; Body mass index more than 32; multi-partnership of the individual or her spouse; chronic systemic diseases including renal failure; hepatic cirrhosis; and cardiovascular diseases; consumption of drugs related to the cardiovascular diseases

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research of Tehran University of Medical Sciences

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