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Evaluation of whether 100 ml of fluid infusion can predict fluid responsiveness in patients with atrial fibrillation

Evaluation of mini-fluid challenge using 100ml of crystalloid as a predictor of fluid responsiveness in patients with atrial fibrillation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0006540
Enrollment
63
Registered
2021-09-03
Start date
2021-07-09
Completion date
Unknown
Last updated
2023-02-08

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

Conditions

None listed

Interventions

None listed

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Adult patients aged 18 to 80 years with atrial fibrillation scheduled for elective surgery that takes more than 1 hour from induction of anesthesia to start of surgery (2) Patients without moderate or more acute/chronic respiratory problems in the pre-operative questionnaire, physical examination, and respiratory examination findings

Exclusion criteria

Exclusion criteria: (1) Patients with moderate or more severe heart valve disease (2) In case of moderate or more obstructive pulmonary disease (COPD grade 2 or higher) (3) Left ventricle ejection fraction < 40% of patients (4) Heart failure patients requiring preoperative inotropics (5) Patients with preoperative blood creatinine levels of 1.3 mg/dL or higher (6) Patients with moderate to severe kidney disease or liver disease (7) Patients with acute lung disease, such as acute lung injury, acute pneumonia, or ARDS (8) Patients who need to maintain spontaneous breathing

Design outcomes

Primary

MeasureTime frame
AUC values for fluid responder prediction of change rate in cardiac output index after 100ml fluid Infusion

Secondary

MeasureTime frame
Gray zone for change rate in cardiac output index after 100ml fluid Infusion

Countries

Korea, Republic of

Contacts

Public ContactAh Ran Oh

Samsung Medical Center

aran8612@gmail.com+82-2-3410-2471

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026