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Withdrawn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
N-methyl-D-aspartate Antagonist (Ketamine) Augmentation of Electroconvulsive Treatment for Severe Major Depression
Terminated
Electroconvulsive therapy (ECT), is considered the most effective treatment for severe treatment resistant major depressive disorder (MDD), but it requires about 3 weeks of treatments and can cause considerable acute deficits in memory. It would be a major advance in treatment if ECT could work faster with fewer treatments and result in decrease incidence of memory problems. Ketamine is an excellent candidate for augmentation of ECT because of its acute effects on depression, its short half-life... Read More
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
04/18/2017
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Major Depressive Disorder
Ketamine Infusion for Treatment-resistant Major Depressive Disorder
Completed
Ketamine infusion has been shown to have rapid antidepressant properties, however the possible use of ketamine in treatment-resistant depression as augmentation has not been investigated. The overall aim of this study is to assess the feasibility, safety and tolerability, efficacy and duration of the effect of intravenous N-methyl-D-aspartate antagonist ketamine as augmentation of antidepressants for chronic suicidal ideation in subjects with severe treatment-resistant depression (TRD). This is... Read More
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
04/18/2017
Locations: Depression Clinical and Research Program - MGH, Boston, Massachusetts
Conditions: Major Depressive Disorder
Ketamine Versus Placebo for Treatment Resistant Major Depressive Disorder
Completed
Ketamine infusions resulted in an acute reduction in global depression scores and in severity of suicidal ideation. The investigators therefore plan to investigate the feasibility and efficacy of repeated intravenous administration of ketamine in severely depressed, treatment resistant patients. The results of the study could lead to development of new strategies for treating depression.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
04/18/2017
Locations: Depression Clinical and Reseach Program - MGH, Boston, Massachusetts
Conditions: Major Depressive Disorder
The Impact of Ketamine on the Reward Circuitry of Suicidal Patients
Withdrawn
Every 40 seconds, someone in the world dies by suicide. There is a lack of effective and safe antisuicidal agents for preventing suicide attempts. This leads to the immense worldwide individual, financial, and societal burden of suicide-which is projected to rise in the coming decades-supporting the need for antisuicidal treatments. This treatment gap may be filled through understanding the neurobiology of suicide, which can guide the development of targeted antisuicidal treatments. Though some... Read More
Gender:
ALL
Ages:
Between 18 years and 85 years
Trial Updated:
03/01/2017
Locations: Massachusetts General Hospital, Boston, Massachusetts
Conditions: Suicidal Ideation, Suicide
Efficacy Study of Ketamine for Postoperative Pain in Opioid Dependent Patients
Completed
Patients who are dependent on opioids often have poor pain relief after major surgery. This study tests the hypothesis that adding intravenous ketamine to a postoperative regimen of intravenous opioids for postoperative pain will improve pain relief in this subset of patients.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
02/01/2017
Locations: Brigham and Women's Hospital, Boston, Massachusetts
Conditions: Postoperative Pain
Safety and Efficacy of PMI-150 (Intranasal Ketamine) for the Treatment of Breakthrough Pain in Cancer Patients
Terminated
To assess the safety and efficacy of PMI-150 (Intranasal Ketamine) as an analgesic for the treatment of breakthrough pain in cancer patients.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
01/10/2012
Locations: Beth Israel Deaconess Medical Center, Boston, Massachusetts
Conditions: Pain, Cancer