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临床试验/NCT03924804
NCT03924804已完成不适用

Effect of Different Infusion Volume on Perioperative Bladder and Blood Volume in Patients Undergoing Daytime Surgery.

China Medical University, China1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2019年6月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
90
试验地点
1
主要终点
1. The change of bladder volume

研究概览

简要总结

The objective of the trial was to explore the effect of different infusion volume on perioperative bladder and blood volume in patients undergoing daytime surgery assisted by bladder and vascular ultrasound and transthoracic echocardiography.

详细描述

The objective of the trial was to evaluate the effects of different infusion volume of Ringer's solution acetate (2 ml/kg,8ml/kg, 16ml/kg) on bladder volume, hemodynamics,transthoracic echocardiography and vascular ultrasound including the inferior vena cava(IVC) and the right subclavian vein(SCV) diameter and the IVC and SCV collapsibility index in patients undergoing daytime surgery through a randomized controlled clinical study, so as to provide better guidance for clinical transfusion avoiding bladder catheterization . The patients in this trial were visited before induction and discharge from the postanaesthesia .We also collected the first time and times of micturition and whether the patients have the dysuria.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ethnic Chinese;
  • age, 18 to 65 years old;
  • American Society of Anaesthesiologists (ASA) physical status I or II;
  • Daytime patients scheduled for general anesthesia

排除标准

  • Patients unwilling to cooperate with the experiment
  • Body mass index exceeding 30 kg/m2;
  • Patients with a history of heart ,liver and Renal failure ,hypertension,diabetes mellitus or arteriosclerosis; and any allergy to drugs used in the study.
  • Patients with the urinary diseases, such as kidney, ureteral calculi and tumors, prostatic hypertrophy.

研究组 & 干预措施

Group C: 16 ml/kg group

Experimental

干预措施: Ringer's solution acetate (Drug)

Group A: 2 ml/kg group

Experimental

干预措施: Ringer's solution acetate (Drug)

Group B: 8 ml/kg group

Experimental

干预措施: Ringer's solution acetate (Drug)

结局指标

主要结局

1. The change of bladder volume

时间窗: baseline and 10 minutes before leaving the post-anesthesia care unite

bladder and blood volume in patients undergoing daytime surgery assisted by bladder and vascular ultrasound

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Wen-fei Tan

Principal Investigator

China Medical University, China

研究点 (1)

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