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Centre Hospitalier Universitaire de Grenoble0 个研究点目标入组 30 人开始时间: 2015年12月3日最近更新: 2019年6月30日

试验速览

暂无简介。

•- Age> 18 years
•- Patients undergoing coronary surgery and / or elective valvular
•- Person affiliated to the social security or receiving such a plan
•- Informed consent in writing signed by the patient or his legal representative.
•- Patients should be operated for cardiac surgery with CPB, in sinus rhythm, and for which the fact of the existence of impaired left ventricular function or the heaviness of the surgical procedure, a decision per Hemodynamic Monitoring and post operative by right heart catheterization is decided.
•- Patient requiring filling of infusion solution
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) no
•F.1.2.1 Number of subjects for this age range 28
•F.1.3 Elderly (>=65 years) no
•F.1.3.1 Number of subjects for this age range 2

•- The persons referred to in Articles 1121-5 to 1121-8 of the CSP: pregnant women, parturient, nursing mother, person deprived of liberty by judicial or administrative decision, person under a legal protection measure
•- Severe pulmonary hypertension (systolic PAP> 60 mmHg)
•- Absence of preoperative sinus rhythm
•- Emergency Surgery
•- Age <18 years
•- Renal impairment dialyzed
•- Severe Hypernatremia (symptomatic, symptomatic associated with sodium and water preoperative overload).

发起方