ISRCTN74508432已完成不适用
Evaluation of a new technology to treat urinary incontinence in women: a single blind randomised controlled trial
Femeda Ltd (UK)0 个研究点目标入组 200 人开始时间: 2011年9月20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
- 200
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
- 性别
- Female
入选标准
- •1. Who suffer from stress incontinence
- •2. Who self refer
- •3. Who are interested in participating in the study
排除标准
- •1. Age under 18 years or more than 65years
- •2. Lack of consent to stimulation
- •3. Pregnancy
- •4. Implanted pacemaker
- •5. Recent pelvic surgery (within last 3 months)
- •6. Recent haemmorhage / haematoma / tissue damage
- •7. Previous or at presently undergoing any active therapy for pelvic malignancy
- •8. Urinary tract infection
- •9. Vaginal infection
- •10. Atrophic vaginitis
- •11. Diabetes or neurological condition
- •12. Any lesions or other pathology of the vagina or labia
- •13. Manual dexterity insufficient to place the device
- •14. Previously had treatment for their urinary incontinence
- •15. Refusal to provide permission for general practitioner (GP) examination
- •16. GP determination that the patient is not suitable for participation in the investigation
- •17. Had baby within the previous 3 months
研究者
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