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Clinical Trials/NCT03089710
NCT03089710CompletedNot Applicable

The Effectiveness of Mini-fluid Challenge in Predicting Fluid Responsiveness During Prone Position Spine Surgery

National Taiwan University Hospital1 site in 1 country100 target enrollmentStarted: March 31, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
Change of cardiac index after fluid loading

Study Overview

Brief Summary

Perioperative fluid management is crucial for patients' outcome. Muller et al developed a "Mini-fluid challenge method " to predict fluid responsiveness and the efficacy. The investigators design the study to investigate the effectiveness of mini-fluid challenge test in prone position surgery.

Detailed Description

Perioperative fluid management is crucial for patients' outcome. Series of studies have indicated that adequate fluid management optimizes the cardiac out put, improves tissue perfusion, thus decrease the risk of postoperative morbidity. Muller et al developed a "Mini-fluid challenge method " to predict fluid responsiveness and the efficacy. To the best of our knowledge, the efficacy of the test was not discussed in the perioperative care in prone position surgery. The investigators design the study to investigate the effectiveness of mini-fluid challenge test in prone position surgery.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
20 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •meet both of
  • •Patients receiving scheduled prone position spine surgery
  • •BMI 18.5~30 kg.m-2

Exclusion Criteria

  • •age younger then 20 yrs or elder than 80 yrs
  • •pregnant women
  • •patients in intensive care units
  • •patients with the underlying disease including respiratory failure(FEV1/FVC < 70 % and FEV1 < 50%), heart failure(NYHA score =III、IV), kidney failure(eGFR< 60 ml.min-1.1.73m-2), liver failure
  • •patients with ongoing infection
  • •patients allergic to voluven

Arms & Interventions

Mini-Fluid Challenge arm

Experimental

Fluid challenge test will be presented after induction of anesthesia at a steady state. Fluid challenge test includes 2 components: 100 ml colloid infusion in 1 min followed by 400 ml colloid infusion in 14 mins. Hemodynamic parameter after 1 minute of the end of the 1st and 2nd colloid infusion bolus will be collected.

Applied colloid: hydroxyethyl starch

Intervention: Mini-fluid challenge (Other)

Outcomes

Primary Outcomes

Change of cardiac index after fluid loading

Time Frame: 3hr

interpretate the correlation of mini-fluid challenge and conventional fluid challenge

Secondary Outcomes

  • pulse pressure variation(PPV)(3hr)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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