TCTR20200723004尚未招募3 期
Effect of different doses of oral Furosemide on Urine volume in peritoNeal Dialysis patients: a randomized controlled trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 100
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
- 年龄范围
- 18 Years 至 80 Years（—）
- 性别
- All
入选标准
- •1. Adults aged 18â€80 years old
- •2. ESRD patients treated with PD at least 1 month
- •3. No history of PD related peritonitis within 1 month
- •4. No history of membrane failure or ultrafiltration failure
排除标准
- •1. Patients with hypotension (mean arterial blood pressure < 65 mmHg) or orthostatic hypotension
- •2. Patients with clinical of fluid overload within 1 month exp. heart failure, generalized edema, pleural effusion or ascites from physical examination or imaging
- •3. Patients who use less than 125 mg or more than 1,000 mg per day of oral furosemide
- •4. Serum potassium less than 3.0 mEq/L
- •5. Serum albumin less than 2.5 g/dL
- •6. Patients using other diuretic drugs
- •7. Patients with contraindication for furosemide
- •8. Patients who have 24-hour urine volume less than 100 ml after the run-in phase of this study
研究者
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