Trials / Completed
CompletedNCT00571441
Estimating Volume Using LiDCO
Estimating Volume Using LiDCO Versus Other Measures of Volume
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 34 (actual)
- Sponsor
- Duke University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
We hypothesize that the stroke volume variation measured using the commercially available LiDCO monitor provides a reasonable estimate of volume when compared to standard measures. This study will collate data that is already being collected by the bedside nurses.
Detailed description
Objective: To compare measurement of stroke volume variance with intake/output measurements, weight, BUN/Creatnine values, and central venous pressure. Design: Non-experimental, non-randomized observational comparative study. Setting: The sixteen bed Neurocritical Care Unit at Duke University Hospital. Patients: 45 adult (over 18 years) subjects with intracranial pathology who require volume resuscitation. Only patients with current LiDCO monitoring will be considered eligible for inclusion in the study. Interventions: This is an observational study. Subjects will receive standard-of-care treatment without additional intervention. Data Analysis: All data will be collected by the principal investigator / study coordinator. Personal patient information will be removed (deidentified) from the permanent data collection records to protect patient confidentiality. Data collected will be entered into a Microsoft Excel electronic spreadsheet and will be saved on a USB Disk drive to be stored in a locked cabinet in the investigator's office. Statistical analysis using SAS v9.1, (Cary, NC) will be conducted with a level of significance set at .05 (alpha) using standardized comparative analysis techniques.
Conditions
Timeline
- Start date
- 2007-12-01
- Primary completion
- 2008-09-01
- Completion
- 2008-12-01
- First posted
- 2007-12-12
- Last updated
- 2016-01-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00571441. Inclusion in this directory is not an endorsement.