CTRI/2018/01/011142已完成3 期
A Randomized Comparative, Open Label, 2 Arm, Phase III Clinical Study to Evaluate the Safety and Efficacy of Vaginal Lubricant for Improvement of Vaginal Dryness
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 40
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
入选标准
- •Women with active sex lives of at least one sexual intercourse in a week
- •Women without a history of sensitivity to similar formulations
- •Subjects willing to sign informed consent and follow the study procedure.
排除标准
- •Women using other intra vaginal gel moisturizer, diagnosed with cancer, Women using hormone replacement therapy in the last 3 months, Absence of history or visible evidence of chronic skin disease or regional infections, genital herpes, vaginal infections or urinary tract infection, Pregnant or lactating, women likely to become pregnant, Personal history of allergy and hypersensitivity to any product of feminine hygiene, severe systemic complications of viral infections, severe systemic illness like cardiovascular disorders, neurological disorders, renal disorders, autoimmune disorders,Not willing to sign informed consent form
研究者
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不适用
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