Status:
UNKNOWN
Use of Integrated Pulmonary Index to Predict Post-Operative Respiratory Adverse Events in High Risk Patients
Lead Sponsor:
Stony Brook University
Conditions:
Postoperative Complications
Eligibility:
All Genders
18+ years
Brief Summary
The Capnostream 20p monitor by Medtronic is FDA-cleared and consists of a monitor which measures real-time respiratory status based on respiratory rate, pulse rate, pulse oximetry (SpO2) and end tidal...
Eligibility Criteria
Inclusion
- 18 years or older Planned to undergo general anesthesia for surgery
Exclusion
- Pregnant Inability to consent Mechanically ventilated prior to surgery
Key Trial Info
Start Date :
September 1 2017
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
September 1 2018
Estimated Enrollment :
600 Patients enrolled
Trial Details
Trial ID
NCT03275324
Start Date
September 1 2017
End Date
September 1 2018
Last Update
September 7 2017
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