Clinical Trials Directory

Trials / Completed

CompletedNCT01477398

Improved Patient Recovery After Anesthesia

Improved Patient Recovery of Spontaneous Respiration After Anesthesia With Hypercapnic Hyperpnoea

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
31 (actual)
Sponsor
University of Utah · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The proposed study will measure the incidence of adverse events and the decrease in time to meet discharge criteria from the post anesthesia care unit when hypercapnic and hyperpnoea are used during emergence.

Detailed description

Hypercapnia has been used in conjunction with hyperpnoea to provide a more rapid return of responsiveness after inhaled anesthesia. The benefits of accelerating patient recovery in the operating room may extend to the post anesthesia care unit if the patient is more alert and easier to care for when they arrive in the unit. Respiratory patterns and gas levels - including CO2, O2, and anesthetic vapor - will be measured in order to better understand a patient's respiratory status during recovery. In Feb 2009 we finished our first study (IRB 26111) and submitted a publication. The journal reviewers identified a serious limitation: we could not report whether the treated patients recovered from anesthesia faster because the treatment (inspired CO2) caused them to breath more vigorously or because the treatment caused the anesthetic vapors to be cleared more rapidly from the brain. Our new application uses essentially the same study protocol as the former study but adds chest bands to measure the patient's rate of breathing and expired gas monitoring to measure the rate at which the vapors are removed.

Conditions

Interventions

TypeNameDescription
DEVICEQED-100Use of the QED-100 results in mild hypercapnia during emergence

Timeline

Start date
2010-04-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2011-11-22
Last updated
2016-08-22

Source: ClinicalTrials.gov record NCT01477398. Inclusion in this directory is not an endorsement.