Clinical Trials Directory

Trials / Completed

CompletedNCT01917526

The Performance of Two Oxygen Delivery Devices Used After General Anesthesia.

The Performance Comparison of Two Oxygen Delivery Devices [Nasal Cannula and Mask] Used After General Anesthesia.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
500 (actual)
Sponsor
Mahidol University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

After general anesthesia, there are the risks for airway obstruction, hypoventilation, atelectasis, ventilation-perfusion mismatch, hypercarbia and hypoxemia,so oxygen supplement in PACU seems necessary. This study aim is to compare the two methods of oxygen supplement which are 1.nasal cannula at O2 flow 4 L/min. 2.oxygen mask with O2 flow 5 L/min. The hypothesis in this study is the 2 methods can equally provide effective oxygen supplement to prevent anesthesia-related hypoxemia. Choosing nasal cannula would be reasonable because it is cheaper and more comfortable to patient.

Detailed description

The incidence and causes of hypoxemia in PACU will be identified, if necessary, a higher flow or changing oxygen delivery system can be used to prevent and treat hypoxemia. If any patients fail from oxygen weaning protocol in PACU and need longer oxygen therapy at ward, the duration of oxygen therapy will be recorded and also the compliance with oxygen delivery devices.

Conditions

Interventions

TypeNameDescription
DEVICEoxygen mask
DEVICEoxygen cannula

Timeline

Start date
2013-04-01
Primary completion
2014-11-01
Completion
2014-12-01
First posted
2013-08-06
Last updated
2017-01-04
Results posted
2017-01-04

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT01917526. Inclusion in this directory is not an endorsement.