Clinical Trials Directory

Trials / Completed

CompletedNCT04701008

Efficacy of Ketamine in Post Anesthesia Recovery Room

Observational Study of the Efficacy of Ketamine for Rescue Analgesia in the Post Anesthesia Recovery Room

Status
Completed
Phase
Study type
Observational
Enrollment
143 (actual)
Sponsor
University of Alberta · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Observational study to assess efficacy of IV ketamine bolus when used in the post anesthesia recovery unit for uncontrolled pain despite use of opioids.

Detailed description

In this observational study, the investigators will monitor all patients with significant pain after any non-cardiac surgical intervention at the University of Alberta Hospital. After receiving an adequate dose of potent opioids (hydromorphone, morphine), the participants will receive up to 0,2-0,25 mg/kg IV ketamine bolus. In our center these boluses are given with 10-20mg increments. The adequate dose of opioids will be determined by the attending anesthesiologist, depending on what patients received intraoperatively and on their comorbidities. Pain scores will be assessed before and after administration of this drug. The incidence of any side effect after ketamine administration will be documented.

Conditions

Interventions

TypeNameDescription
DRUGKetamineIV ketamine - 10mg bolus may be repeated repeated 2-3 times depending on clinical judgement

Timeline

Start date
2020-09-01
Primary completion
2021-05-28
Completion
2021-05-28
First posted
2021-01-08
Last updated
2024-09-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT04701008. Inclusion in this directory is not an endorsement.