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Clinical Trials/NCT03924804
NCT03924804
Completed
Not Applicable

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

China Medical University, China1 site in 1 country90 target enrollmentJune 19, 2019

Overview

Phase
Not Applicable
Intervention
Ringer's solution acetate
Conditions
Cholecystolithiasis and Thyroid Nodule
Sponsor
China Medical University, China
Enrollment
90
Locations
1
Primary Endpoint
1. The change of bladder volume
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

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.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
June 19, 2019
End Date
May 12, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wen-fei Tan

Principal Investigator

China Medical University, China

Eligibility Criteria

Inclusion Criteria

  • ethnic Chinese;
  • age, 18 to 65 years old;
  • American Society of Anaesthesiologists (ASA) physical status I or II;
  • 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.

Arms & Interventions

Group C: 16 ml/kg group

Intervention: Ringer's solution acetate

Group A: 2 ml/kg group

Intervention: Ringer's solution acetate

Group B: 8 ml/kg group

Intervention: Ringer's solution acetate

Outcomes

Primary Outcomes

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

Study Sites (1)

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