Open Study of the Neurobiological Effects of Intranasal Ketamine in Children and Adults With Bipolar Disorder
Unknown
Aim 1: Test the hypothesis that participants with Bipolar Disorder - Fear of Harm Phenotype have an enhanced amygdala fMRI response to fearful threatening stimuli, increased resting beta and gamma EEG spectral activity in temporal leads and blunted posterior insula response to cold when partially withdrawn from ketamine with normalization of these responses following intranasal administration of ketamine. Aim 2. Test the hypothesis that ketamine alters response to fearful-threatening visual sti... Read More
Gender:
ALL
Ages:
Between 14 years and 40 years
Trial Updated:
01/26/2022
Locations: McLean Hospital, Belmont, Massachusetts
Conditions: Bipolar Disorder
The PATHFINDER Study: A Feasibility Trial
Completed
The main purpose of this study is to determine whether a rational strategy of EEG guided multimodal general anesthesia using target specific sedative and analgesics could result in enhanced recovery after anesthesia and surgery, decrease in postoperative delirium, and decrease in long term postoperative cognitive dysfunction up to 6 months following cardiac surgery.
Gender:
ALL
Ages:
60 years and above
Trial Updated:
01/27/2021
Locations: Beth Israel Deaconess Medical Center, Boston, Massachusetts
Conditions: Coronary Artery Disease, Delirium
EEG Studies of Ketamine General Anesthesia
Completed
We are doing this research study to find out how and where ketamine acts in the brain. Ketamine is an anesthetic (a drug or agent used to decrease or eliminate the feeling of pain by putting you in an unconscious state). We will look at the brain using a machine that records the brain's electrical activity, called an electroencephalogram (EEG). We will assess how it impacts patient's pain responses.
Gender:
ALL
Ages:
Between 18 years and 45 years
Trial Updated:
08/14/2020
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Anesthesia
Effect of Ketamine on Opioid-Induced Hyperalgesia
Completed
The purpose of this study is to compare pain threshold, pain tolerance, and wind up, as measured by QST, before and after a single dose of ketamine infusion under two clinical conditions: chronic pain patients on opioid therapy and chronic pain patients without opioid therapy.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
07/21/2020
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Pain, Chronic Pain, Hyperalgesia
A Study of Brexpiprazole Plus Ketamine in Treatment-Resistant Depression (TRD)
Completed
This is a multi-site, double-blind, placebo-controlled study of the acute efficacy of brexpiprazole or placebo in combination with intranasal ketamine added to ongoing, stable, and adequate antidepressant therapy (ADT) in the treatment of adults with Major Depressive Disorder with Treatment Resistant Depression.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
07/16/2020
Locations: Massachusetts General Hospital, Depression Clinical and Research Program, Boston, Massachusetts
Conditions: Depression
EEG Studies of Sevoflurane-Induced General Anesthesia
Completed
The investigators are performing this research study to find out how and where the anesthetic drugs sevoflurane and ketamine act in the brain. Sevoflurane and ketamine are anesthetics (a drug or agent used to decrease or eliminate the feeling of pain by causing unconsciousness). The investigators will study the brain using a machine that records the brain's electrical activity, called an electroencephalogram (EEG).
Gender:
ALL
Ages:
Between 18 years and 50 years
Trial Updated:
10/01/2019
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Anesthesia
Ketamine for Major Depressive Disorder
Unknown
The purpose of this study is to measure the amount of ketamine in blood over time in subjects diagnosed with Major Depressive Disorder (MDD) and explore the anti-depressive effects of ketamine delivered by transdermal patch.
Gender:
ALL
Ages:
Between 18 years and 70 years
Trial Updated:
04/24/2019
Locations: Clinical Research Site, Boston, Massachusetts
Conditions: Major Depressive Disorder
Ketamine for Depression: An MRI Study
Completed
Ketamine has been shown to decrease symptoms of anxious depression quickly. This decrease has been shown to last for up to one month. MRI technology will be used before and after ketamine for patients with depression to examine the extent to which certain brain areas predict ketamine's antidepressant effects.
Gender:
ALL
Ages:
Between 18 years and 64 years
Trial Updated:
04/03/2019
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Depression, Anxious Depression, Major Depressive Disorder
Double-Blind, Placebo-Controlled Trial of Ketamine Therapy in Treatment-Resistant Depression (TRD)
Completed
This study is looking at the efficacy, durability, safety, and tolerability of multiple single doses of Ketamine vs. active placebo for treating patients with treatment resistant depression who are taking an antidepressant that is not working for them.
Gender:
ALL
Ages:
Between 18 years and 70 years
Trial Updated:
05/24/2018
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Treatment Resistant Depression
Physiological and Cognitive Biomarkers for Ketamine's Antidepressant Effects
Terminated
Anxious depression is a particularly difficult-to-treat subtype of depression. Patients with anxious depression do not respond as well to currently available antidepressant medications. Nevertheless, in previous studies, low dose IV ketamine, which rapidly decreases symptoms of depression within hours in many patients with "treatment-resistant" depression, has been associated with superior efficacy in those individuals with anxious compared with non-anxious depression. In order to understand thi... Read More
Gender:
ALL
Ages:
Between 18 years and 64 years
Trial Updated:
03/22/2018
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Depression
Ketamine and Scopolamine Infusions for Treatment-resistant Major Depressive Disorder
Withdrawn
Ketamine infusions resulted in an acute reduction in global depression scores and in severity of suicidal ideation. Scopolamine infusions produced also a significant improvement in depression that was sustained over time. We therefore plan to investigate the feasibility and efficacy of open-label repeated intravenous administration of ketamine and scopolamine combined in this population of severely depressed, treatment-resistant patients. The results from this study could lead to the developmen... Read More
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
02/15/2018
Locations: Depression Clinical and Reseach Program - MGH, Boston, Massachusetts
Conditions: Major Depressive Disorder
Immunomodulatory Properties of Ketamine in Sepsis
Completed
The aim of the study is to assess the effect of short-term infusion of ketamine at analgesic dosage on the immune response, morbidity and mortality among patients suffering from septic shock. We hypothesize that ketamine will modulate the cytokine response to sepsis and reduce morbidity and mortality.
Gender:
ALL
Ages:
Between 21 years and 100 years
Trial Updated:
07/21/2017
Locations: Beth Israel Deaconess Medical Center, Boston, Massachusetts
Conditions: Sepsis