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Ketamine for Dissociative Symptoms
Phase 1
Recruiting
Led By Karl Deisseroth, MD, PhD
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Age >18 years old.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 1 week
Awards & highlights
All Individual Drugs Already Approved
Approved for 5 Other Conditions
No Placebo-Only Group
Summary
This trial will investigate how ketamine causes dissociative symptoms by looking at how it affects the brain.
Who is the study for?
This trial is for adults over 18 with epilepsy who are in the Stanford Epilepsy Monitoring Unit. It's not suitable for those who can't communicate in English, are pregnant or nursing, have had bad reactions to ketamine before, or have a history of psychotic or bipolar disorders.
What is being tested?
The study focuses on understanding how ketamine may cause dissociative symptoms among epilepsy patients. Participants will receive ketamine under controlled conditions while their responses and experiences are closely monitored.
What are the potential side effects?
Ketamine can lead to side effects such as feeling disconnected from reality (dissociation), changes in perception, confusion, agitation, drowsiness, increased blood pressure and heart rate.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am older than 18 years.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 1 week
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 1 week
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Number of participants with dissociative events during ketamine infusion as assessed by CADSS (Clinician-Administered Dissociative State Scale)
Awards & Highlights
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 5 Other Conditions
This treatment demonstrated efficacy for 5 other conditions.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: KetamineExperimental Treatment1 Intervention
Study participants will receive 0.5mg/kg of ketamine - one single infusion
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ketamine
FDA approved
Find a Location
Who is running the clinical trial?
Stanford UniversityLead Sponsor
2,469 Previous Clinical Trials
17,501,727 Total Patients Enrolled
16 Trials studying Epilepsy
1,203 Patients Enrolled for Epilepsy
Karl Deisseroth, MD, PhD1.01 ReviewsPrincipal Investigator - Stanford University
Stanford University
1 Previous Clinical Trials
120 Total Patients Enrolled
1Patient Review
I was very uncomfortable around him. He was dismissive of my concerns about side effects and just increased the dosage. He spoke to me in a condescending way and made personal and sexual accusations. I would not recommend him to anyone.
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have had a bad reaction to ketamine before.I am older than 18 years.I am a patient in the Stanford Epilepsy Monitoring Unit.You have been diagnosed with a serious mental health condition like schizophrenia or bipolar disorder at any point in your life.
Research Study Groups:
This trial has the following groups:- Group 1: Ketamine
Awards:
This trial has 3 awards, including:- All Individual Drugs Already Approved - Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
- Approved for 5 Other Conditions - This treatment demonstrated efficacy for 5 other conditions.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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