IRCT20121031011341N11招募中3 期
The efficacy of Fumaria parviflora L. versus gabapentin on uremic pruritus of patients undergoing hemodialysis: A randomized non-inferiority double-blinded active-controlled clinical trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 70
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 60 years（—）
- 性别
- All
入选标准
- •The hemodialysis patient who has uncontrollable pruritus and now at least 1 week doesn't use any antipruritus medication
- •who had pruritus for at least 6 weeks
- •patient must have normal range phosphor and potassium in the past month
- •Parathyroid Hormone (PTH) must be lower than 500
- •measured visual analogue scale (VAS) score must be four or more
排除标准
- •They do not have liver disease, a history of convulsions, or a specific skin disease that causes itching, and they do not have hemolytic blood disease.
- •Patients who complain of itching for the first time are not included in the study
- •If the patient was taking medication that interacted with gabapentin or Fumaria parviflora L., he was not included in the study
- •Those who are allergic to Fumaria parviflora L. or Gabapentin are not included in the study
研究者
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