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Clinical Trial Summary

Primary:

The purpose of this study is to assess the clinical implications of continuous distal CO2 monitoring when used for clinical decisions

Sub Study:

• Evaluate the average life time (duration) of Standard Carinal VitaLine set in comparison to the Carinal VitaLine set that its sampling tubing is made of PEBAX (dehumidifying material).

Description of Study Design:

Patients will be randomized at the baseline evaluation visit into one of the following groups:

- Masked group: Data derived from the Capnostream20p will be recorded; however the medical staff will be masked from it and hence will not use it.

- Open group: Data derived from the Capnostream20p and displayed to the medical team. It will allow the treating physician and the nursing team to review the real time data and make clinical decisions based upon it if felt necessary.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Intubated Neonates That Require Conventional Ventilation

NCT number NCT01572272
Study type Observational
Source Medtronic - MITG
Contact
Status Completed
Phase N/A
Start date August 2012
Completion date February 2015