Clinical Trials Directory

Trials / Completed

CompletedNCT01700907

Optimization of Desflurane in Elderly Patients

Optimization of Desflurane in Elderly Patients Compared With Sevoflurane: A Pilot Study

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Sapporo Medical University · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

Various issues had been pointed out when undergoing the anesthesia for elderly patients with sevoflurane, such as delayed emergence, post-operative trouble with swallowing. Desflurane, which has a lower blood/gas partition coefficient, is expected to contribute the better emergence, along with the recent progress on optimization of delivered amount of anesthesia. The purpose of this study is to compare the time to emergence in long elderly patient cases with desflurane or sevoflurane, with the recently developed drug-delivery optimization system "Aisys®" (GE Healthcare Japan).

Detailed description

The objectives of this study is to compare the time to emergence and quality of recovery in long elderly patient cases with desflurane or sevoflurane, with the recently developed drug-delivery optimization system "Aisys®" (GE Healthcare Japan). Inclusion Criteria: \- Elderly patients (\>= 65 yr-old), long operation (\> 4hours), abdominal surgery patients Exclusion Criteria: \- Liver dysfunction, Renal dysfunction, preoperative dementia Neurosurgery patients, Cardiac surgery patients, obese patients(BMI\>35)

Conditions

Interventions

TypeNameDescription
DRUGDesfluraneThe patients in this arm will be given the general anesthesia with desflurane and be used the Aysis as the anesthetic machine.
DRUGSevofluraneThe patients in this arm will be given the general anesthesia with sevoflurane and be used the Aysis as the anesthetic machine.

Timeline

Start date
2012-08-01
Primary completion
2013-02-01
Completion
2013-02-01
First posted
2012-10-04
Last updated
2014-11-27
Results posted
2014-11-27

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT01700907. Inclusion in this directory is not an endorsement.