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Clinical Trial Summary

A prospective cohort pilot study of non-cardiac patients to determine the feasibility of recruiting 150 patients to undergo postoperative continuous hemodynamic monitoring for up to 3 days.


Clinical Trial Description

Patient will start wearing the Philips' hemodynamic and ECG monitor in the Post Anaesthesia Care Unit (PACU). This device will continuously measure heart rate, pulse oxymetry, and ST-segments. The device will measure blood pressure every hour from 7 am to 10 pm and every 2 hours from 10 pm to 7 am.

Patients will have postoperative Troponin I monitoring and telephone follow-up at 30 days postop. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02300441
Study type Observational
Source McMaster University
Contact
Status Completed
Phase
Start date September 2014
Completion date September 2015