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A clinical trial to study the use of a new monitoring modality(stroke volume variation using Flotrac/Vigileo) for predicting the need for fluids in patients on artificial ventilation

Evaluation of stroke volume variation as predictor of fluid responsiveness using pulse contour analysis device (Flotrac/Vigileo) in mechanically ventilated patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2010/091/000442
Enrollment
26
Registered
2010-05-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Administration of intravenous fluids to patients undergoing major surgery based on monitoring of stroke volume variation and compare it with CVP and systolic pressure variation monitoring

Interventions

Intervention1: Preloading with 6% Hydroxyethylstarch 7ml/kg: Measurement of stroke volume variation using Flotrac/Vigileo,Systolic pressure variation and central venous pressure Control Intervention1:

Sponsors

Department of Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I or II patients scheduled for any major surgery requiring invasive monitoring

Exclusion criteria

Exclusion criteria: a) Patients with known cardiac disease b) Patients with pre-operative arrhythmia c) Patients with severe COPD or other respiratory disorder d) Patients with known peripheral vascular disease/Modified Allen?s test positive. e) Severe coagulopathy

Design outcomes

Primary

MeasureTime frame
To evaluate whether stroke volume variation obtained by (FlotracTM/VigileoTM) can predict fluid responsiveness in mechanically ventilated patients.Timepoint: Befor preloading and after preloading—

Secondary

MeasureTime frame
To compare the predictive value of stroke volume variation obtained by (FlotracTM/VigileoTM) with those of other preload indices such as systolic pressure variation and central venous pressure.Timepoint: Before preloading and after preloading—

Countries

India

Contacts

Public ContactRavi Raj

Department of Anaesthesiology,All India Institute of Medical Sciences, Ansari Nagar,New Delhi

drraviraj2007@gmail.com08591666981

Outcome results

None listed

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