EUCTR2018-002715-10-ES进行中（未招募）1 期
RANDOMIZED, DOUBLE-BLIND, PILOT CLINICAL TRIAL TO COMPARE THE EFFICACY AND SAFETY OF FISH OIL-BASED INTRAVENOUS LIPID EMULSIONS IN HOSPITALIZED ADULT PATIENTS TREATED WITH TOTAL PARENTERAL NUTRITION WITH HYPERTRIGLYCERIDEMIA
Elisabet Leiva Badosa. Phamacy Department. Hospital Universitari de Bellvitge0 个研究点目标入组 30 人开始时间: 2018年11月16日最近更新:
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
- 30
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
入选标准
- •1. Subjects must be 18 years of age or older and may be of both genders and of any race / ethnicity.
- •2. Subjects must be willing to give written informed consent for the trial and be able to do. Otherwise, it can be done by the legal representative.
- •3. Subjects should have triglyceride levels between 3 and 4.5 mmol / L and have been treated for at least 1 day with NP.
- •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 15
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 15
排除标准
- •1. Subjects may not have a history of type I hypersensitivity or idiosyncratic reactions to any component of lipid emulsions.
- •2. Women who are pregnant or breast-feeding.
- •3. Subjects treated with propofol
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