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 ventilatio
Not Applicable
Completed
- 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
- Registration Number
- CTRI/2010/091/000442
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 26
Inclusion Criteria
ASA I or II patients scheduled for any major surgery requiring invasive monitoring
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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