EUCTR2017-002169-23-DK进行中（未招募）1 期
The effect of clinical characterization of children with monosymptomatic nocturnal enuresis on the efficacy of desmopressin and alarm therapy. - DRYCHILD
Søren Rittig0 个研究点目标入组 400 人开始时间: 2017年6月30日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Age 6-14 years.
- •2. Three or more wet nights per week regarding the home registrations.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 400
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Ongoing constipation and/or faecal incontinence.
- •2. Daytime symptoms such as urgency, frequency or incontinence.
- •3. Recurrent urinary tract infections.
- •4. Anamnestic, clinical or laboratory findings that can be related to diseases or conditions that might affect the parameters investigated.
- •5. Neurological and/or known clinically significant anatomical abnormalities of the urinary tract.
- •6. Former operations in the urinary tract.
- •7. Prior or ongoing treatment with alarm, desmopressin or anticholinergics.
- •8. Ongoing medication that may interfere with the parameters tested.
- •9. Pregnant or lactating girl.
- •10. Contra-indications for the use of desmopressin: habitual or psychogenic polydipsia, use of diuretics, renal insufficiency, hyponatraemia or SIADH.
- •11. Hypersensitivity / allergy to substances in the tablets.
研究者
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