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

NCT03924804 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2022-05-13

No results posted yet for this study

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.

Conditions

  • Cholecystolithiasis and Thyroid Nodule

Interventions

DRUG

Ringer's solution acetate

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

DRUG

Ringer's solution acetate

Intravenous infusion of 8ml/kg Ringer's solution acetate within 1 hour after induction.

DRUG

Ringer's solution acetate

Intravenous infusion of 16ml/kg Ringer's solution acetate within 1 hour after induction.

Sponsors & Collaborators

  • China Medical University, China

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-19
Primary Completion
2022-05-12
Completion
2022-05-12

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03924804 on ClinicalTrials.gov