Clinical Trials Directory

Trials / Completed

CompletedNCT01463527

Using Capnography to Reduce Hypoxia During Pediatric Sedation

Using Capnography to Reduce the Incidence of Hypoxia in Children During Moderate Sedation in the Pediatric Emergency Department: A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
167 (actual)
Sponsor
Yale University · Academic / Other
Sex
All
Age
1 Year – 20 Years
Healthy volunteers
Not accepted

Summary

The investigators hypothesize that the addition of capnography during moderate sedation will improve recognition of hypoventilation and apnea. This will lead to an increased frequency of staff interventions such as verbal or physical stimulation for these events in order to improve ventilation which will in turn lead to a reduction in the frequency of oxygen desaturations. If capnography proves to be effective in creating earlier detection and intervention for hypoventilation and apnea during moderate sedation provided by non-anesthesiologists, this device can be used in a variety of clinical settings to enhance patient safety.

Conditions

Interventions

TypeNameDescription
DEVICENellcor NPB-70 CapnographUse of capnography as an additional monitor during sedation to detect hypoventilation and apnea prior to declines in pulse oximetry and clinical examination findings

Timeline

Start date
2011-09-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2011-11-02
Last updated
2018-01-11
Results posted
2014-08-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01463527. Inclusion in this directory is not an endorsement.