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Evaluating the Accuracy of a Skin-Attached Ultrasound Device (EdgeFlow CW10) in Predicting the Need for Fluid Administration During Abdominal Surgery

The evaluation of estimated stroke volume variation derived from EdgeFlow CW10 as a predictor of fluid responsiveness in patients undergoing laparotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0012292
Enrollment
38
Registered
2026-07-16
Start date
2026-08-03
Completion date
Unknown
Last updated
2026-07-20

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: Male or female aged 19 to 90 years Patients undergoing abdominal surgery with radial artery catheterization Patients who voluntarily provide written informed consent after receiving a full explanation of the study

Exclusion criteria

Exclusion criteria: Patients with carotid artery vascular disease (atherosclerosis or stenosis, history of stent insertion, or history of bypass surgery) Patients with arrhythmia Patients with left ventricular ejection fraction less than 40% Patients with right ventricular dysfunction or intracardiac shunt Patients with moderate or greater cardiac, pulmonary, hepatic, or renal disease Patients requiring preoperative inotropic support Patients with an open thorax Patients with spontaneous breathing

Design outcomes

Primary

MeasureTime frame
Area under the ROC curve (AUC) of estimated stroke volume variation (eSVV) for predicting fluid responsiveness

Secondary

MeasureTime frame
Comparison of AUC between eSVV from EdgeFlow CW10 and SVV from AcumenIQ sensor;Change in estimated stroke volume variation (eSVV) before and after fluid administration;Change in stroke volume (SV) before and after fluid administration;Change in stroke volume variation (SVV) before and after fluid administration;Change in cardiac output (CO) before and after fluid administration;Correlation between estimated stroke volume variation (eSVV) and stroke volume variation (SVV);Incidence of device-related adverse events

Countries

Korea, Republic of

Contacts

Public ContactJoon-suk Bom

Samsung Medical Center

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

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Jul 23, 2026