IRCT20231003059605N1已完成1 期
COMPARISON OF ORAL VERSUS INTRAVENOUS IRON THERAPY IN IMPROVING HEMOGLOBIN STATUS IN PATIENTS OF CHRONIC KIDNEY DISEASE
Pak Emirates Military Hospital Rawalpindi0 个研究点目标入组 210 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 210
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 no limit（—）
- 性别
- All
入选标准
- •Inclusion criteria included all male and female patients over the age of 18 years
- •Not on hemodialysis or erythropoietin diagnosed as anemia with a baseline Hb of less than 13 g/dl in males and less than 12 g/dl in females
- •With established chronic kidney disease with a GFR (glomerular filtration rate) of less than 60ml/min for more than 90 days assessed using the CKD-EPI equation and/or hyper albuminuria with urine albumin ? 30 mg in 24 hours or urine albumin to creatinine ratio (ACR) ? 30 mg/g.
排除标准
- •Exclusion criteria included patients on dialysis, erythropoietin or use of erythropoietin stimulating agents (ESAs) in the last 3 months
- •Patients with advanced liver, cardiac or ESKD (end-stage kidney disease)
- •Drug allergies to iron and its supplemental form during therapy or previous known history
- •Unwilling to be included in the study.
研究者
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