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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06252207
Other study ID # 23-1049
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 1, 2024
Est. completion date December 1, 2025

Study information

Verified date May 2024
Source The Cleveland Clinic
Contact Sandra A Durbin, CLPN, CCRP
Phone 216-269-4073
Email DURBINS3@ccf.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators thus propose a comparative effectiveness quality improvement project to evaluate the feasibility of switching from near-exclusive use of isoflurane in adult general surgical patients to Desflurane.


Description:

The three available volatile anesthetics appear to be comparably safe. However, higher solubility slows emergence from isoflurane and sevoflurane compared to Desflurane. Even a few minutes delay in emergence from anesthesia has financial implications since institutional costs of operating room time can easily be $30 per minute. Postoperative care is also expensive. Furthermore, in busy hospitals such as the Cleveland Clinic, inadequate recovery throughput frequently delays surgery. The investigators thus propose a comparative effectiveness quality improvement project to evaluate the feasibility of switching from near-exclusive use of isoflurane in adult general surgical patients to Desflurane. (The investigators will exclude children because there are compelling clinical reasons to use sevoflurane in pediatric patients.) The proposed comparison is between isoflurane (our current routine) and Desflurane which is no longer used at the Clinic because of price concerns - a decision that that did not consider down-stream effects, including prolonged emergence and recovery.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 2619
Est. completion date December 1, 2025
Est. primary completion date March 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adults having general anesthesia in the G operating room suite at the Cleveland Clinic Main Campus. Exclusion Criteria: - Operations lasting <1.5 hours.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Desflurane
General anesthesia with desflurlane
Isoflurane
General anesthesia with isoflurane

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The Cleveland Clinic

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of post-anesthesia care unit recovery Time from entry to the post-anesthesia to discharge from unit. 1 hour
Secondary Duration of anesthetic emergence Time from a MAC fraction of 0.3 (presumably shortly after volatile anesthesia is discontinued) and extubation. 1 hour
Secondary Cost of post-anesthesia care unit. Cost of post-anesthesia unit care. To be estimated only if there is a substantial difference between the groups. 2 hours
Secondary Delirium Incidence of postoperative delirium. 5 days
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