Observational and Minimal Interventional Study Designed to Collect Data During Planned Surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Elective, Non-thoracic, Open surgical procedures
- Registration Number
- CTRI/2015/03/005657
- Lead Sponsor
- ellcor Puritan Bennett LLC Doing Business as Covidien
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 75
Inclusion Criteria
• Adult patient >= 18 years of age scheduled for an elective, open non-thoracic surgical procedure.
• Expected duration of the surgical procedure to be >= 1.5 hours.
• Expected radial artery cannulation and ECG monitoring in the Operating Room.
• Measurement of Invasive Blood Pressure via Radial cannulation site
Exclusion Criteria
Patients with active cardiac arrhythmia, indwelling intra-aortic balloon pump, Left Ventricular assist device, undergoing thoracic open surgery, having history of severe contact allergies to adhesive material e.g. pulse oximetry sensors etc, skin lesions or deformities on fingers and forehead, pregnant female and vulnerable patients.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method