Ketamine in Patients Undergoing TEVAR Procedures Receiving NCI
Brief Summary
Condition or Disease
- Descending Aortic Dissection
- Postoperative Pain
- Thoracoabdominal Aortic Aneurysm
Phase
Study Design
Study type: | Interventional |
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Status: | Not yet recruiting |
Study results: | No Results Available |
Age: | 18 Years to 90 Years (Adult, Older Adult) |
Enrollment: | 20 () |
Funded by: | Other |
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Clinical Trial Dates
Start date: | Oct 20, 2020 | |
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Primary Completion: | Aug 01, 2022 | |
Completion Date: | Aug 01, 2022 | |
Study First Posted: | Oct 23, 2020 | |
Last Updated: | Oct 23, 2020 |
Sponsors / Collaborators
Location
Patients undergoing descending aortic repair often experience post-operative pain, and have high post operative opioid requirements. That pain is partially due to the use of naloxone continuous infusion (NCI). NCI is part of a bundled approach used in the first 48 hours post-operatively to prevent spinal cord ischemia, a devastating complication associated with surgical repair of the descending aortic. Data indicate that patients receiving NCI experience elevated post-operative pain scores and increased opioid requirements during the 48-hr post-operative NCI administration, compared to patients not receiving NCI.
Ketamine is an FDA-approved N-methyl D-aspartate (NMDA) antagonist that has been shown to provide adjunctive analgesia and opioid-sparing effects in post-operative surgical patients. At low doses, ketamine provides analgesic benefit without the anesthetic effects seen at higher doses. These doses are commonly referred to sub-dissociative. This study will evaluate whether use of sub dissociative ketamine (SDK) in patients undergoing aortic procedures with the use of NCI will lead to decreased post-operative opioid consumption, and produce improved pain scores in the first 48 hours.
Eligibility Criteria
Sex: | All |
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Minimum Age: | 18 |
Maximum Age: | 90 |
More Details
NCT Number: | NCT04600089 |
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Acronym: | 2020Ketamine |
Other IDs: | 60617 |
Study URL: | https://ClinicalTrials.gov/show/NCT04600089 |