EUCTR2021-006789-19-PL招募中1 期
Efficacy comparison of two doses of vitamin D3 in critically ill patients undergoing continuous renal replacement therapy - NephroD - NephroD
SK w Opolu0 个研究点目标入组 138 人开始时间: 2022年2月11日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 138
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
- All
入选标准
- •1. Presence of at least one of the following indications for implementation of CRRT by CVVHDF or CVVHF (Clinical Practice Guideline for Acute Kidney Injury):
- •- replacement of non-functioning kidney function when acute kidney injury occurs
- •- hyperkalemia
- •- metabolic acidosis
- •- pulmonary edema
- •- complications of uremia (hemorrhagic diathesis, pericarditis)
- •- hypervolaemia
- •- Renal function support (control of goiter, acid-base, ion balance)
- •2. organ failure score (SOFA) of at least 5 at the time of qualification for the study
- •3. patient age >18 years
- •4. 25(OH)D3 serum concentration =12.5 ng/ml - test performed by the local laboratory of the participating hospital
- •5. Properly managed enteral nutrition (through a gastric tuber or orally) at any dose.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 138
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 138
排除标准
- •1. acute or advanced chronic liver failure (estimated by clinical presentation and biochemical markers: serum bilirubin, serum AST and ALT, high AST/ALT serum ratio, glycemia, INR value)
- •2. hypercalcemia (total calcium >11 mg/dL or >2,7mmol/L )
- •3. Any parathyroid disease
- •4. KDIGO classification of end-stage renal disease
- •5. Patients undergoing plasmapheresis, extracorporeal membrane oxygenation (ECMO), extracorporeal carbon dioxide elimination (ECCO2R)
- •6. Patients who, in the opinion of the investigator, do not have a good chance of surviving the 72 hour period after study entry
- •7. history of kidney stones or de novo renal calculi
- •8. patient eligible for futile therapy avoidance protocol
- •9. pregnancy
- •10. sarcoidosis
- •11. risk of impaired intestinal absorption in critical illness associated with at least one of the mentioned: impaired intestinal motility and delayed gastric emptying, constipation, diarrhea, intestinal hypoperfusion in shock, intoxication with subsequent intestinal edema after fluid resuscitation, changes in the intestinal microbiome.
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