Brain wave test may reveal if your antidepressant is working
NCT ID NCT00792168
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether brain wave patterns (measured by QEEG) can predict how well people with major depression respond to the antidepressant venlafaxine (Effexor). Thirty-eight adults with depression received either venlafaxine or a placebo for a short time, then continued with open-label treatment. Researchers monitored brain activity and depression symptoms to see if early brain changes could forecast later improvement.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- venlafaxine (Effexor)
- What this could lead to
- If successful, this could help doctors use brain wave patterns to quickly tell if an antidepressant is working, potentially speeding up treatment decisions for depression.
- What could go wrong
- This is a small, early-phase study with only 38 participants, so results may not apply to everyone. The brain wave test (QEEG) is still experimental and not a proven tool for guiding treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
38 people
The number who actually took part.
- Started
-
Nov 1996
- Finished
-
Dec 1998
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All subjects will meet DSM-IV criteria for depression on the basis of a SCID-P interview, with subjects in the placebo controlled phase of the study having a score on the 17-item Ham-D \> 18 (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. Exclusion Criteria: * 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 * 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 placebo-controlled phase of the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of California
Los Angeles, California, 90024, United States
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Other studies related to the condition(s) this trial covers.
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