CTIS2024-511517-38-00进行中（未招募）1 期
A prospective randomized, single-blind, multicenter phase II study comparing two methods of cardioplegia in cardiac surgery due to congenital heart malformation in children: Custodiol-N versus Custodiol (CL-N-CP-Paed-II/09/19) - CL-N-CP-Paed
Dr. Franz Koehler Chemie GmbH0 个研究点目标入组 100 人开始时间: 2024年5月15日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 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
- 0 至 17（—）
- 性别
- All
入选标准
- •Age from birth to less than 18 years of age, congenital heart surgery with cardiopulmonary bypass and cardioplegia, written informed consent of the patients and/ or their legal guardians (must be available before enrolment in the study), Ability of the legal guardians to understand character and individual consequences of the clinical trial
排除标准
- •Patients who have participated within 30 days or are still participating in any other interventional study, History of severe organic (e.g. liver or kidney) disease other than concerning the heart, History of psychiatric disease, Pregnancy and lactation
研究者
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