CYP2B6 Polymorphisms in Ketamine
NCT01988922 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2018-05-18
Summary
This research study will determine if genetic variation in CYP2B6 affects how the body metabolizes ketamine.
Conditions
- Healthy Volunteers
Interventions
- DRUG
-
0.4 mg/kg oral racemic ketamine
Sponsors & Collaborators
-
Washington University School of Medicine
lead OTHER
Principal Investigators
-
Lesley Rao, MD · Washington University School of Medicine
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2013-11-30
- Primary Completion
- 2016-05-31
- Completion
- 2017-05-31
Countries
- United States
Study Locations
More Related Trials
-
Blood Sampling for Neurochemical and Genetic Testing
NCT00001147 ·Status: COMPLETED
-
Genetic Predictors of Lithium Response in Bipolar Disorder
NCT00252577 ·Status: COMPLETED
-
Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2
NCT01193088 ·Status: RECRUITING
-
Pharmacogenomics of Antidepressant Response in Children and Adolescents
NCT00516932 ·Status: COMPLETED
-
Genetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway
NCT03799705 ·Status: COMPLETED
-
Patient and Provider Confidence and Satisfaction With the Clinical Use of CYP Genetic Variability
NCT02568618 ·Status: TERMINATED ·Phase: EARLY_PHASE1
-
Reverse Phenotyping Core
NCT03632239 ·Status: ENROLLING_BY_INVITATION
-
Primary Hyperoxaluria Mutation Genotyping
NCT00589225 ·Status: COMPLETED
-
Genetics of Primary Ciliary Dyskinesia
NCT02389049 ·Status: COMPLETED
-
Genetics of Epilepsy and Related Disorders
NCT01858285 ·Status: RECRUITING
-
Genotype and Phenotype Registry: Enrollment of Normal Control Subjects for Current and Future Research
NCT00926042 ·Status: COMPLETED
-
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders
NCT04399694 ·Status: COMPLETED
-
CABP2 Patient Registry and Natural History Study
NCT06680934 ·Status: RECRUITING
-
Study of Clinical and Molecular Manifestations of Genetic Disorders
NCT00001466 ·Status: COMPLETED
-
Analyzing Genes That May Increase the Risk of Developing High Blood Pressure
NCT00549991 ·Status: COMPLETED
-
Screening of Healthy Adults for Genetic Variations That Control Fatty Acid Processing
NCT01516125 ·Status: COMPLETED
-
Pharmacogenetic Testing and Chronic Pain
NCT05259865 ·Status: SUSPENDED
-
Characterization of Phenotypic and Genotypic Regressors for Imaging
NCT01148381 ·Status: COMPLETED
-
Study of Genetic Differences in People With Depression
NCT00229463 ·Status: COMPLETED
-
Genetics of Hepatitis C Virus Infection
NCT00005657 ·Status: COMPLETED
-
Cause and Pathogenesis of Neurometabolic Disorders
NCT00016562 ·Status: COMPLETED
-
Studies of Children With Metabolic and Other Genetic Disorders
NCT00025870 ·Status: COMPLETED
-
Characterization of Dysmorphology in Subjects With Creatine Transporter Deficiency
NCT05600946 ·Status: RECRUITING
-
Exome Sequencing in Autistic Spectrum Disorder
NCT01059201 ·Status: COMPLETED
-
Use of Population Descriptors in Human Genetic Research
NCT00767702 ·Status: COMPLETED