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临床试验/TCTR20180118003
TCTR20180118003尚未招募3 期

Effect of short-course oral ciprofloxacin on the pharmacokinetics of isoflavones in healthy postmenopausal women

Faculty of Medicine, Chiang Mai University0 个研究点目标入组 12 人开始时间: 2018年1月18日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
12

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
46 Years 至 0 N/A (No limit)(—)
性别
Female

入选标准

  • Aged >45 years with postmenopausal status >1 years and serum follicle-stimulating hormone (FSH) concentration >40 IU/L, the body mass index (BMI) must be within 18-25 kg/m2. Subjects are in good health based on medical history and physical examination.

排除标准

  • Subjects with abnormal hematological diseases or impaired kidney or liver function. Subjects with known contraindication or hypersensitivity to soy isoflavones or ciprofloxacin will be excluded as well as those with history of malignancy, cardiovascular, pulmonary, or breast disease. History of musculoskeletal diseases such as arthralgia or back pain, joint stiffness, achiness, neck or chest pain, and flare up of gout. Other exclusion criteria include a history of cigarette smoking, substance abuse or addiction, regular consumption of alcohol-containing beverages, and use of antibiotics and laxative within the previous 4 weeks.

研究者

发起方
Faculty of Medicine, Chiang Mai University

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