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临床试验/NCT01449305
NCT01449305已完成不适用

Research on Effectiveness of Nanoone Woman Underwear Using in the Management of Dysmenorrhea

Chen Yi Enterprise, Co., Ltd.1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2011年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
44
试验地点
1
主要终点
The Mean Change in Maximum Pain Level at Each Menstrual Cycle From Baseline

研究概览

简要总结

To evaluate the mean change in menstrual pain intensity during menstrual cycles from baseline after wearing Nanoone Woman Underwear in women with primary dysmenorrhea

详细描述

The severity of dysmenorrhea pain experienced by subjects will be evaluated on a VAS, ranging from zero (no pain) to ten (very severe pain). Subjects will be asked to use the VAS scoring system to record, on a provided sheet, their experienced menstrual pain level daily during menstrual bleeding for a total of three consecutive menstrual cycles.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
13 Years 至 40 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Females aged below 40 years old.
  • Screened by inquiry and diagnosed as primary dysmenorrhea by gynaecologist with pelvic ultrasonography.
  • Female subject who is:
  • using adequate contraception since last menstruation and no plan for conception during the study.
  • non-lactating.
  • has negative pregnancy test (urine) within 14 days prior to the study.
  • Informed consent form signed.

排除标准

  • Sensitivity to study product.
  • Patient has been diagnosed with secondary dysmenorrhea (defined as identifiable pelvic pathology).
  • Patient has clinically significant physical disability or abnormal findings on physical examination or laboratory testing judged by the investigator or co-investigator.
  • Participation of any clinical investigation during the last 30 days.

结局指标

主要结局

The Mean Change in Maximum Pain Level at Each Menstrual Cycle From Baseline

时间窗: baseline, first menstrual cycle, second menstrual cycle and third menstrual cycle

The severity of dysmenorrhea pain experienced by subjects will be evaluated on a VAS, ranging from zero (no pain) to ten (very severe pain).

次要结局

未报告次要终点

研究者

发起方
Chen Yi Enterprise, Co., Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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