DRKS00029349招募中未知
Improvement of different menopausal symptoms under the use of the nutritional menopausal product Exelvit Menopausia - Menoxel -1
Chemo Group0 个研究点目标入组 160 人开始时间: 2022年6月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 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
- 分配方式
- N/a: Single Arm Study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 50 Years 至 90 Years(—)
- 性别
- Female
入选标准
- •1. Female patients, age = 50 years and being menopausal according to clinical symptoms
- •2. FSH (> 50 mIU/mL) and Estradiol (< 30 pg/mL)
- •3. Written informed Consent
排除标准
- •1. Current BMI > 35 kg/m2
- •2. Patients with severe acute or chronic diseases (e.g. pancreatitis, hypertriglyceridemia, liver disease, malign or benign tumor of the liver, malign sex-hormone-dependent diseases of the genital or the breast)
- •3. Migraine with Aura
- •4. Intake of drugs, which induce microsomal enzymes, especially cytochrome-P450, e.g. phenytoine, phenobarbital, pyrimidon, bosentan, carbamazepin, rifampicin, topiramate, felbamate, griseofulvine, some HIV protease inhibitors (e.g. ritonavir) und non-nucleosidic inhibitors of reverse transciptase (e.g. efavirenz) and androgen receptor (AR) antagonists (e.g. enzalutamide).
- •5. History of cardiocascular disease
- •6. Advanced high blood pressure or diabetes mellitus
- •7. Existence or known risk for venous or arterial thromboembolism
- •8. Non-diagnosed abnormous vaginal bleeding
- •9. Use of drugs containing Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir during the study period and two weeks in advance
- •10. Pregnancy and Breast feeding during the study period
- •11. Allergy to one of the compounds of the product
- •12. Concomitant use of other nutritional products or female sexual hormones during the study and 8 weeks before
研究者
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