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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03089710
Enrollment
100
Registered
2017-03-24
Start date
2017-03-31
Completion date
2018-09-14
Last updated
2020-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

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.

Interventions

Mini-fluid challenge test with 100mL colloid infusion in 1 min

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

meet both of 1. Patients receiving scheduled prone position spine surgery 2. BMI 18.5\ 30 kg.m-2

Exclusion criteria

1. age younger then 20 yrs or elder than 80 yrs 2. pregnant women 3. patients in intensive care units 4. 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 5. patients with ongoing infection 6. patients allergic to voluven

Design outcomes

Primary

MeasureTime frameDescription
Change of cardiac index after fluid loading3hrinterpretate the correlation of mini-fluid challenge and conventional fluid challenge

Secondary

MeasureTime frameDescription
pulse pressure variation(PPV)3hrinterpretate the correlation of PPV and conventional fluid challenge

Other

MeasureTime frameDescription
stroke volume variation(SVV)3hrinterpretate the correlation of SVV and conventional fluid challenge
plethysmographic variation index(PVI)3hrinterpretate the correlation of PVI and conventional fluid challenge

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026