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

KetamineDepressionAnesthesia

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

This trial is not recruiting

This study is currently not accepting new participants.

Find recruiting trials
Data Source
ClinicalTrials.gov

Last updated from source