Neuroimaging of St. John's Wort-Induced Changes of Serotonin Metabolism in Normal Subjects
NCT00001919 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 13
Last updated 2008-03-04
Summary
St. John's Wort is a popular dietary supplement that many people take to elevate mood or relieve stress. This study will test in normal volunteers whether this preparation may alter mood and if so, by what means. Animal studies suggest that St. John's Wort may work similarly to some antidepressants that affect levels of the chemical serotonin in the brain.
Participants in this study must also be enrolled in NIMH protocol #98-M-0094 (SPECT Imaging of Dopamine and Serotonin Transporters in Neuropsychiatric Patients and Normal Volunteers) and protocol #91-M-014 (MRI Imaging of Neuropsychiatric Patients and Controls). Separate consent forms are required for each study. Candidates will undergo medical and psychiatric evaluations that may include blood and urine tests, electroencephalogram and electrocardiogram.
Normal volunteers will have a mood assessment at the beginning of the study. They will then be randomly assigned to take either placebo (a pill with no active ingredient) or St. John's Wort 3 times a day for 2 weeks, and will be told what they are taking. After an 11-week hiatus, they will again start treatment on the same schedule, but will not be told which preparation they are receiving. Each evening during the 2-week treatment periods, subjects will complete a brief self-rating mood assessment questionnaire. At the end of each treatment period, they will undergo SPECT brain imaging (a type of CT scan) to determine dopamine and serotonin distribution and density in the brain.
For this procedure, study subjects take three drops of potassium iodide solution within 24 hours before the scan and two drops nightly for 3 days following the procedure. About 10 ml (less than two teaspoons) of blood are drawn before a radioactive tracer is injected. SPECT imaging is done the next day. After about 1 hour of imaging, subjects are given either a placebo or St. John's Wort, and then imaging continues for another 2 hours. During the procedure, up to five blood samples of 6 ml each may be drawn. At some point during the study, a MRI scan of the brain will be done.
Conditions
- Healthy
- Mood Disorder
Interventions
- DRUG
-
Hypericum (LI-160)
Sponsors & Collaborators
-
National Institute of Mental Health (NIMH)
lead NIH
Eligibility
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 1999-09-30
- Completion
- 2002-06-30
Countries
- United States
Study Locations
More Related Trials
-
Examination of Brain Serotonin Receptors in Patients With Mood Disorders
NCT00026832 ·Status: COMPLETED
-
St. John's Wort And Kava In The Treatment Of Major Depressive Disorder With Comorbid Anxiety
NCT00451516 ·Status: COMPLETED ·Phase: PHASE2
-
Sertraline Compared With Hypericum Perforatum (St.John's Wort) in Treating Depression
NCT00066859 ·Status: COMPLETED ·Phase: PHASE3
-
The Role of Dopamine Metabolism in the Antidepressant Effects of Sleep Deprivation and Sertraline in Depressed Patients
NCT00581009 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Double Blind Randomized, Monocentric, Cross-over, Placebo-controlled Study to Evaluate the Effect of Citalopram on Motivation
NCT02113943 ·Status: COMPLETED ·Phase: PHASE2
-
Chinese Herb for the Treatment of Depression and Anxiety Disorders
NCT03323697 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Human Cerebral Blood Flow and Serotonin
NCT05957094 ·Status: UNKNOWN ·Phase: NA
-
Rhodiola Rosea Therapy of Major Depressive Disorder
NCT01098318 ·Status: COMPLETED ·Phase: PHASE3
-
Modulation of Visually Evoked Potentials by an Antidepressant
NCT00263133 ·Status: COMPLETED ·Phase: NA
-
Sensoril(Ashwaganhda)for Bipolar Disorder
NCT00761761 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of Seltorexant as Adjunctive Therapy to Antidepressants in Adult and Elderly Participants With Major Depressive Disorder With Insomnia Symptoms Who Have Responded Inadequately to Antidepressant and Long-term Safety Extension Treatment With Seltorexant
NCT04533529 ·Status: COMPLETED ·Phase: PHASE3
-
A Controlled Trial of Serotonin Reuptake Inhibitors Added to Stimulant Medication in Youth With Severe Mood Dysregulation
NCT00794040 ·Status: COMPLETED ·Phase: PHASE2
-
Serotonin and Everyday Social Interaction
NCT02051569 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Citalopram to Enhance Cognition in HD
NCT00271596 ·Status: COMPLETED ·Phase: PHASE2
-
Effects of Cognitive Behavioral Therapy on Brain Serotonin Activity in People With Depression
NCT00641108 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Treatment of Citalopram for Anxiety Disorders Following a Traumatic Brain Injury
NCT00208572 ·Status: UNKNOWN ·Phase: NA
-
A Study of Seltorexant as Adjunctive Therapy to Antidepressants in Adult and Elderly Participants With Major Depressive Disorder With Insomnia Symptoms Who Have Responded Inadequately to Antidepressant Therapy
NCT04532749 ·Status: TERMINATED ·Phase: PHASE3
-
Mood Effects of Serotonin Agonists Extended
NCT03934710 ·Status: COMPLETED ·Phase: PHASE1
-
The Metabolic Effects of Antidepressants in Patients Diagnosed With Major Depressive Disorder
NCT01418638 ·Status: UNKNOWN
-
Brain Response to Serotonergic Medications in ASD
NCT04145076 ·Status: UNKNOWN ·Phase: NA
-
Sertraline and Cognitive Therapy in Depressed Alcoholics
NCT00000458 ·Status: COMPLETED ·Phase: PHASE2
-
A Retrospective And Multicenter Survey To Investigate The Dosage, Efficacy And Safety Of Sertraline In Posttraumatic Stress Disorder Patients
NCT01607593 ·Status: COMPLETED
-
7T Amygdala and Citalopram Study
NCT06412315 ·Status: RECRUITING ·Phase: NA
-
Serotonin Function During Depression
NCT00033787 ·Status: COMPLETED
-
Management Strategy for Mild to Moderate Major Depression: Combination of Rhodiola and Saffron Extracts.
NCT02981225 ·Status: COMPLETED