Skip to content

The Effectiveness of Mini-fluid Challenge in Predicting Fluid Responsiveness During Video Assisted Thoracic Surgery

The Effectiveness of Mini-fluid Challenge in Predicting Fluid Responsiveness During Video Assisted Thoracic Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03731377
Enrollment
100
Registered
2018-11-06
Start date
2020-10-07
Completion date
2021-11-30
Last updated
2020-10-08

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

Conditions

Mini-fluid Challenge in Video-Assisted Thoracic Surgery

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 video assisted thoracic 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. Fluid status and proper perfusion condition in patients undergo thoracic surgery are especially crucial for the vulnerability of lung toward fluid overload. To the best of our knowledge, the efficacy of the test was not discussed in the perioperative care in video assisted thoracic surgery. The investigators design the study to investigate the effectiveness of mini-fluid challenge test in video assisted thoracic surgery.

Interventions

Mini-fluid challenge with crystalloid 250 ml will be given to patients first. After observation of hemodynamic parameters, further fluid challenge will be given for response observation.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients receiving scheduled video assisted thoracic 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 * patient allergic to voluven

Design outcomes

Primary

MeasureTime frameDescription
Change of blood pressure after fluid loading3 hoursInterpretate the correlation of mini-fluid challenge and conventional fluid challenge

Secondary

MeasureTime frameDescription
Change of cardiac index after fluid loading3 hoursInterpretate the correlation of mini-fluid challenge and conventional fluid challenge

Other

MeasureTime frameDescription
stroke volume index(SVI)3 hoursInterpretate the correlation of mini-fluid challenge and conventional fluid challenge
stroke volume variation(SVV)3 hoursInterpretate the correlation of mini-fluid challenge and conventional fluid challenge
pulse pressure variation(PPV)3 hoursInterpretate the correlation of mini-fluid challenge and conventional fluid challenge
plethysmographic variation index(PVI)3 hoursInterpretate the correlation of mini-fluid challenge and conventional fluid challenge
stroke volume (SV)3 hoursInterpretate the correlation of mini-fluid challenge and conventional fluid challenge

Countries

Taiwan

Contacts

Primary ContactTzu Jung Wei
sa46222@gmail.com+886972653416
Backup ContactNational Taiwan University Hospital

Outcome results

None listed

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