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临床试验/NCT01635231
NCT01635231已完成不适用

Effect of Thiazide, Amiloride and Hypertonic Saline on Sodium- and Water Channel Activity in the Nephron in Healthy Subjects Estimated by Urinary Biomarkers

Regional Hospital Holstebro1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2012年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
24
试验地点
1
主要终点
urinary biomarkers

研究概览

简要总结

Urinary biomarkers (u-NKCC2, u-ENaC-gamma and u-AQP2) reflects the activity of the sodium- and water channels in the human kidney.

Changes in the sodium-and water channel activity can be induced by blocking the sodium channels with diuretics in healthy subjects

详细描述

  1. Urinary biomarkers (u-NKCC2, u-ENaC-gamma and u-AQP2) reflects the kidneys transport of sodium and water in the nephron.
  2. Changes in the sodium-and water channel activity is induced by blocking the NCC channels with thiazide and ENaC channels with amiloride and by intervention with hypertonic NaCl The changes in sodium-and water channels are followed by changes in extracellular and intracellular fluids, central bloodpressure and the plasma concentration of vasoactive hormones.

The purpose of this study is to investigate the changes in urinary biomarkers (u-NKCC2, u-ENaC-gamma and u-AQP2), extra- and intracellular fluid compartments, central bloodpressure and the plasma concentration of Vasoactive hormones in healthy subjects under a) treatment with Amiloride and Thiazide at baseline and b) after and acute infusion with hypertonic saline.

Subjects will be examined on three examination days. Four days prior to the examination days the subjects will consume a standard diet based on amount of sodium and calories and randomized to treatment with either thiazide, amiloride or placebo twice daily for 5 days. On the examination days the subjects receive an infusion with hypertonic saline.

Renal function is measured by renal clearance of 51Cr-EDTA. Urinary biomarkers (u-NKCC2, u-ENaC-gamma and u-AQP2) will be measured to evaluate the activity of water- and sodium channels in the nephron, changes in fluid compartments are measured by body composition monitor. Central blood pressure is measured by sphygmocor.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •healthy males and females
  • •age 18-45
  • •BMI range 18,5-30,0 kg/m2

排除标准

  • •hypertension (i.e. ambulatory BP > 130 mmHg systolic or/and > 80 mmHg diastolic)
  • •history or clinical significant signs of heart, lung, liver, kidney, endocrine, brain or neoplastic
  • •alcohol abuse
  • •drug abuse
  • •pregnancy or nursing
  • •blood donation within a month prior to examination
  • •medical treatment apart from oral contraception abnormal blood samples, -ECG and -urine dipstick, drug abuse, alcohol abuse, pregnancy, medication

研究组 & 干预措施

thiazide, diuretic

Active Comparator

1.25 mg thiazide twice daily for 5 days

干预措施: hypertonic saline (Other)

amiloride, diuretic

Active Comparator

5 mg of amiloride twice daily

干预措施: hypertonic saline (Other)

calcium

Placebo Comparator

placebo twice daily for 5 days

干预措施: hypertonic saline (Other)

结局指标

主要结局

urinary biomarkers

时间窗: baseline, 0 hours and 1.5 hours after intervention

Urinary excretion of epithelial sodium channels (ENaC), Sodium-potassium-2chloride transporters (NKCC2) and aquaporin2 channels (AQP2) before, during and after fluid infusion

次要结局

  • vaso active hormones(baseline, 0 hours and 1.5 hours after intervention)
  • central blood pressure(baseline, 0 hours and 1.5 hours after intervention)
  • intracellular (ICV)- and extracellular volume (ECV)(baseline, 0 hours and 1.5 hours after intervention)

研究者

发起方
Regional Hospital Holstebro
申办方类型
Other
责任方
Principal Investigator
主要研究者

Erling Bjerregaard Pedersen

Ph.d student Janni Majgaard Jensen

Regional Hospital Holstebro

研究点 (1)

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