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Completed

NCT Number: NCT03924804

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

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

the First Hospital of China Medical University

Shenyang, Liaoning, 110001, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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.

Treatment and study plan

Ringer's solution acetate

Drug

Intravenous infusion of 2 ml/kg Ringer's solution acetate within 1 hour after induction.

Primary outcomes

  1. 1. The change of bladder volume

    Time frame: 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

Sponsors and collaborators

Lead sponsor

China Medical University, China

Other

Registry information

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Apr 23, 2019
Registry last updated
May 13, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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