UnknownPhase 4ketamine
Ketamine Co-induction for Patients With Major Depressive Disorder
Sponsored by University of Saskatchewan
NCT ID
NCT03666494
Target Enrollment
50 participants
Start Date
2018-12
Est. Completion
2019-12
About This Study
Ketamine hydrochloride, an anesthetic medication, has been demonstrated to acutely and rapidly improve depressive symptoms but not yet been adequately studied for this effect when used as part of a general anesthetic for surgery. This proposed single-centre, double-blinded, randomized clinical trial of adult patients with depression presenting for gynecologic surgery would compare severity of depressive symptoms between patients receiving and not receiving ketamine as part of their general anesthetic.
Conditions Studied
Interventions
- •Ketamine Hydrochloride
- •Propofol
- •Fentanyl
Eligibility
Sex:FEMALE
Age:18 Years - 65 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * Diagnosis of major depressive disorder * Presentation for gynecologic surgery requiring a general anesthetic Exclusion Criteria: * Marked co-morbid cardiovascular disease * Marked co-morbid respiratory disease * History of intracranial hypertension * History of seizures * ASA Physical Status Classification IV or greater * History of psychosis * Current pregnancy * Contraindication to ketamine administration