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
| Type | Name | Description |
|---|---|---|
| DRUG | Ketamine | IV 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.