Comparing Ketamine and Propofol Anesthesia for Electroconvulsive Therapy
Information source: University of Saskatchewan
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Treatment Resistant Depression
Intervention: Propofol (Drug); Ketamine (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: University of Saskatchewan Official(s) and/or principal investigator(s): Jonathan Gamble, MD, Principal Investigator, Affiliation: University of Saskatchewan
Overall contact: Jonathan Gamble, MD, Phone: 1-306-655-1183, Email: J_Gamble@yahoo.com
Summary
To determine the effect of ketamine, compared to propofol, when used an an anesthetic agent
for electroconvulsive therapy (ECT) in the treatment of major depressive disorder (MDD). We
hypothesize that ketamine, compared to propofol, will improve the the symptoms of MDD when
used as the anesthetic agent to facilitate ECT. Additionally, we hypothesize the
dissociative and cardiovascular effects of ketamine will be minimal.
Clinical Details
Official title: A Prospective Randomized Double Blinded Control Trial Using Ketamine or Propofol Anesthesia for Electroconvulsive Therapy: Improving Treatment-Resistant Depression
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: The primary outcome is defined as the number of ECT treatments required to reach a 50% reduction in baseline MADRS (Montgomery-Asberg Depression Scale) score.
Secondary outcome: Change in CADSS (Clinician Administered Dissociative States Scale)Change in ALS-18 (Affective Lability Scale) Change in ECT energy settings and seizure quality Hemodynamic instability and respiratory complications Time to discharge Change in MADRS score
Detailed description:
Treatment resistant depression is a common and disabling condition. The delayed onset of
action and side effects exhibited by oral antidepressants are significant limitations. An
alternative and well-established therapy is electroconvulsive therapy (ECT). ECT has rapid
antidepressant effect beginning with the completion of the first session. Nevertheless,
like oral medications, patients treated with ECT can develop treatment resistance or failure
to respond. There is great need for a novel approach to treatment-resistant depression; one
that that is safe, has rapid onset, and is sustained.
Pharmaceutical agents with rapid antidepressant effects are a new and promising paradigm in
the research for treatment of MDD. A potential therapeutic target is glutamate based signal
transmission because glutamate transmission is abnormally regulated in the limbic/cortical
areas of many depressed people. Glutamatergic modulating agents, in particular ketamine,
have been shown to induce rapid antidepressant effects both in both preclinical models and
humans. Additionally, ketamine has been shown to have persistent antidepressive effect.
Presently worldwide, propofol is one of the most commonly used anesthetic agents for ECT.
There are 2 main disadvantages to this practice. First, propofol has no antidepressive
effect. Second, propofol is a potent anticonvulsant that may worsen the quality of the ECT
induced seizures. A recent open-label trial compared ketamine to propofol for anesthesia
during ECT and demonstrated a significant improvement of depression in the ketamine arm.
Ketamine is routinely used to provide safe general anesthesia as well as procedural
sedation, analgesia, and amnesia. The combination of the intrinsic antidepressant effects of
ketamine with electroconvulsive therapy is a promising concept in clinical research.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Fulfill the diagnostic criteria for major depression according to the Diagnostic and
Statistical Manual of Mental Disorders (most recent edition)
- Failure to respond to at least 2 adequate drug therapies for the current depression
episode
- MADRS score of 20 or above (moderate - severe
- ASA physical status classification I to III
Exclusion Criteria:
- Inability to obtain informed consent
- ASA physical status classification IV
- Complication by any serious physical diseases such as cardiovascular disease
(including untreated HTN), respiratory disease, cerebrovascular disease, intracranial
HTN (including glaucoma), or seizures
- Presence of foreign body (including pacemaker)
- Pregnancy
- Allergies to anesthetics used in study Includes: a) Ketamine b) Propofol c) Eggs d)
Egg products e) Soybeans f) Soy products
Locations and Contacts
Jonathan Gamble, MD, Phone: 1-306-655-1183, Email: J_Gamble@yahoo.com
Royal University Hospital, Saskatoon, Saskatchewan S7N 0W8, Canada; Recruiting Jonathan Gamble, MD, Principal Investigator
Additional Information
Related publications: Zarate CA Jr, Singh JB, Carlson PJ, Brutsche NE, Ameli R, Luckenbaugh DA, Charney DS, Manji HK. A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression. Arch Gen Psychiatry. 2006 Aug;63(8):856-64. Berman RM, Cappiello A, Anand A, Oren DA, Heninger GR, Charney DS, Krystal JH. Antidepressant effects of ketamine in depressed patients. Biol Psychiatry. 2000 Feb 15;47(4):351-4. Zarate CA Jr, Brutsche NE, Ibrahim L, Franco-Chaves J, Diazgranados N, Cravchik A, Selter J, Marquardt CA, Liberty V, Luckenbaugh DA. Replication of ketamine's antidepressant efficacy in bipolar depression: a randomized controlled add-on trial. Biol Psychiatry. 2012 Jun 1;71(11):939-46. doi: 10.1016/j.biopsych.2011.12.010. Epub 2012 Jan 31. Diazgranados N, Ibrahim L, Brutsche NE, Newberg A, Kronstein P, Khalife S, Kammerer WA, Quezado Z, Luckenbaugh DA, Salvadore G, Machado-Vieira R, Manji HK, Zarate CA Jr. A randomized add-on trial of an N-methyl-D-aspartate antagonist in treatment-resistant bipolar depression. Arch Gen Psychiatry. 2010 Aug;67(8):793-802. doi: 10.1001/archgenpsychiatry.2010.90. Okamoto N, Nakai T, Sakamoto K, Nagafusa Y, Higuchi T, Nishikawa T. Rapid antidepressant effect of ketamine anesthesia during electroconvulsive therapy of treatment-resistant depression: comparing ketamine and propofol anesthesia. J ECT. 2010 Sep;26(3):223-7. doi: 10.1097/YCT.0b013e3181c3b0aa. Wang X, Chen Y, Zhou X, Liu F, Zhang T, Zhang C. Effects of propofol and ketamine as combined anesthesia for electroconvulsive therapy in patients with depressive disorder. J ECT. 2012 Jun;28(2):128-32. doi: 10.1097/YCT.0b013e31824d1d02.
Starting date: September 2013
Last updated: April 22, 2014
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