Study of the Effects of an Antidepressant Medication and Placebo on the Brain Functioning of Normal Subjects

University of California, Los Angeles (UCLA)

Status and phase

Completed

Phase 4

Conditions

Depression

Treatments

Drug: venlafaxine

Study type

Interventional

Funder types

Other

Identifiers

NCT00634283

07-10-051

Details and patient eligibility

About

This study examines the effects of an antidepressant medication and placebo on the brain functioning of normal subjects. In this study, recordings of brain electrical activity are being used to detect and monitor the response to treatment with venlafaxine IR (Effexor), a drug used for the treatment of depression. The intent of this study is to test specific hypotheses regarding:

long-term brain effects of a single course of antidepressant treatment
pharmaco-conditioning effects underlying antidepressant tolerance/sensitization
brain functional response to initial versus subsequent antidepressant trials in normal healthy subjects.

Full description

Major Depressive Disorder (MDD) is a lifelong and recurrent illness, such that many individuals require multiple courses of antidepressant medication treatment. While some patients respond completely to each course of treatment, many do not, and with each unsuccessful antidepressant trial the likelihood that a patient will respond decreases. This raises the possibility that neurophysiologic response in subsequent antidepressant treatment may be influenced by learning processes including sensitization, habituation, and/or classical conditioning. Classical conditioning would entail the association of cues such as pill-taking (conditioned stimuli; CS) with the effects of active medication (unconditioned stimulus; US), such that later presentation of the CS alone would come to elicit a conditioned response (CR). Such effects could be revealed by blinded administration of placebo following a period of treatment with active medication. Habituation effects (tolerance), or sensitization effects (increased response), which require only repeated exposure to a stimulus, might be evidenced after repeated courses of antidepressant treatment. Knowledge of how learning processes impact neurophysiologic response to successive courses of antidepressant treatment would have relevance for clinical populations. Specific hypotheses, however, may be tested in healthy non-clinical samples to avoid potential confounding factors related to severity or chronicity of illness. Learning theories would suggest two hypotheses: (1) neurophysiologic response to placebo will differ between subjects who were previously treated with antidepressant treatment as compared to placebo (classical conditioning hypothesis); and (2) neurophysiologic response to an initial course of antidepressant treatment will differ from response to a repeated course of antidepressant treatment.

Enrollment

6 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subject age is 18-75 years
Subject must be in overall good health (i.e., free of any medical condition known to affect brain function).
Subject must have participated in former study, Physiologic Monitoring of Antidepressant Medication Effects in Normal Controls Subjects (IRB#: 00-11-038-13)
Subject has had a normal physical exam within one year prior to entry of the study
Capacity to give Informed Consent

Exclusion criteria

Subject has serious medical illness, such as high blood pressure, heart disease, renal impairment, or cirrhosis of the liver.
Subject meets DSM-IV Axis I criteria for a mood, anxiety, cognitive, or psychiatric disorder; or meets criteria for cluster A or B axis II diagnoses. These disorders will be determined on the basis of a structured assessment with the MINI (Mini International Neuropsychiatric Interview for DSM-IV Axis I Disorders)
Subject has a history of current or past active suicidal ideation or suicide attempts.
Subject has received treatment with an antidepressant medication or any medications that could influence brain function since his/her participation in the initial study
Subject is using any of the following medications which interfere with EEG measures of brain function: Anticholinergics, Barbiturates, Benzodiazepines, Sedating Antihistamines (e.g. diphenhydramine (Benadryl) would be exclusionary, but not loratadine (Claritin))
Subject has a history of seizures, brain surgery, skull fracture, significant head trauma, or previous abnormal EEG
Subject is pregnant or planning on becoming pregnancy during course of the study
Subject is a UCLA student or staff member directly under instruction or employment of any of the investigators