Electroencephalography (EEG) Biomarkers of Response in Depression
Completed · Phase 4 · Has a placebo group
Conditions studied: Major Depressive Disorder
In brief
There are two specific aims of this project: 1. To identify physiologic indicators of venlafaxine treatment response using quantitative EEG (QEEG) cordance, and to determine if cordance changes are specifically associated with response to venlafaxine 2. To identify predictors of placebo response in major depression using QEEG cordance/bispectral index (BIS) and neuropsychological testing
Key facts
- Study ID
- NCT00759122
- Run by
- University of California, Los Angeles
- People needed
- 44
- Starts
- 2002-11-01
- Expected to finish
- 2005-12-01
- Last updated by the study team
- 2008-09-25
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All subjects will meet DSM-IV criteria for depression on the basis of a SCID-P interview, with subjects having a score on the 17-item Ham-D > 17 (with item #1 > 2).
- Subjects will meet criteria both at recruitment and after a one-week single blind placebo wash-in. Study includes outpatients only.
You may not qualify if…
- All subjects will have no serious medical illness. The investigators will exclude patients also meeting criteria for the following groups of axis I diagnoses:
- delirium or dementia
- substance-related disorders
- schizophrenia or other psychotic disorders, or eating disorders.
- In addition, patients meeting criteria for cluster A or B axis II diagnoses will be excluded.
- Subjects with a history of current or past active suicidal ideation, or suicide attempts will be excluded from the study.
Where it is running
- UCLA Laboratory of Brain, Behavior, and Pharmacology — Los Angeles, California, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.