Ketamine in Patients Undergoing TEVAR Procedures Receiving NCI

Recruiting Phase 2 Interventional Study
Descending Aortic Dissection Postoperative Pain Thoracoabdominal Aortic Aneurysm
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 90
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
Sam Tyagi · Other
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About This Trial

The objective of this study is to identify the opioid-sparing effects, and pain-reduction potential of low dose, sub-dissociative ketamine on patients undergoing thoracic endovascular aortic repair (TEVAR) procedures receiving naloxone continuous infusion (NCI).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * willing to give informed consent * scheduled for elective thoracic aorta repair or thoracoabdominal aortic repair * requires naloxone continuous infusion for spinal prophylaxis Exclusion Criteria: * allergy to ketamine, acetaminophen, or fentanyl * diagnosis of schizophrenia…
Contacts

Eric Johnson, PharmD

8593235722

eric.johnson@uky.edu

CONTACT