Clinical Trials Directory

Trials / Unknown

UnknownNCT03783676

Does Precise Delivery of Remifentanil Decrease Coughing at Emergence From Anesthesia

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
University of Vermont Medical Center · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

The investigators want to find a way to reduce or stop patients from coughing at the end of surgery when the breathing tube is taken out. The breathing tube is removed when the participants are waking up from anesthesia, and are at the point when the participants can breathe on your own. In most types of surgery, coughing at this point is common, and does not affect the participants very much, if at all. But for surgery involving the eye or the head and neck, coughing right after surgery can cause bleeding at the site of surgery. This study will use a short-acting pain drug called remifentanil at the end of surgery to prevent coughing. The investigators will give the participants this medicine for 5 to 30 minutes. The point of the study is to test if using a simple computer program to guide precise delivery of how much of the drug is given to the participants is effective at reducing or preventing coughing.

Conditions

Interventions

TypeNameDescription
DRUGRemifentanilReceive remifentanil bolus and infusion guided by an algorithm.
DRUGNormal salineReceive normal saline bolus and infusion guided by the remifentanil algorithm.

Timeline

Start date
2019-02-15
Primary completion
2019-06-01
Completion
2019-06-01
First posted
2018-12-21
Last updated
2018-12-24

Regulatory

Source: ClinicalTrials.gov record NCT03783676. Inclusion in this directory is not an endorsement.