Validation of the methodology of serum creatinine measurement and the estimated glomular filtration ratio - URIS

niversity Hospital Ghent0 个研究点目标入组 30 人开始时间: 2006年2月7日最近更新: 2014年10月7日

适应症

试验速览

暂无简介。

•The subjects are adult volunteers participating in the study after an informed consent.
•Subjects who meet all of the following criteria are eligible for this trial:
•1. Aged between 18 and 55 years.
•2. Normal weight as defined by a Body Mass Index of 18 to 30 kg/m2.
•3. Subject is competent and willing to sign informed consent form after being given all the detailed information about the study. Informed consent form signed voluntarily.
•4. The subjects must be in stable clinical condition, with stable serum creatinin at least for 6 months.
•5. Persons with different stage of chronic renal disease and without kidney disease (living donors) who need an evaluation of the GFR or Admitted volunteers who easily obtain urine samples.
•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
•F.1.3 Elderly (>=65 years) no
•F.1.3.1 Number of subjects for this age range

•Subjects meeting one or more of the following criteria cannot be selected:
•1. Transplant patients
•2. Medication that will influence the serumcreatinine.
•3. Morbid obesity
•4. Pregnant, lactating females or females with childbearing potential without adequate contraception (use of oral contraceptives, IUD or condoms with spermicide).
•5. History of allergy or hypersensitivity to inulin
•6. Donation of blood in the 60 days preceding the first visit.
•7. Liver disease, heart failure, nephrotic syndrome.
•8. Patients in critically ill conditions.
•9. Malnutrition
•10. Postrenal kidney failure

发起方

niversity Hospital Ghent