Clinical exploratory study on the usefulness of hemodynamic preloading parameters using noninvasive cardiac output measuring device (ClearSight) for perioperative fluid management
Not Applicable
- Conditions
- Biliary tumor, pancreatic tumor, and esophageal tumor
- Registration Number
- JPRN-UMIN000025497
- Lead Sponsor
- Hokkaido Universtiy Graduate School of Medicine, Department of Gastroenterological SurgeryII
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 18
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients with Peripheral Arterial Occlusive Disease 2. Patients with chronic arrhythmia 3. Patients with high risk of postoperative delirium 4. Investigator could exclude insufficient patients for this study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method