Atlanta, Georgia 30322

  • Major Depressive Disorder

Purpose:

The primary objective of this project is to determine whether treatment with the SSRI, fluoxetine versus placebo reverses alterations in the central CRF system induced by early life stress experiences (i.e. childhood sexual and/or physical abuse) in cases with and without major depression. We also evaluate whether neuroendocrine changes after SSRI treatment correlate with clinical improvement.


Study summary:

We compare indices of central CRF activity (i.e. ACTH and cortisol response to CRF stimulation test) before and after 8 weeks of treatment with either fluoxetine or placebo between women with a history of childhood abuse (early life stress, ELS) and current major depression (ELS/MDD), women with a history of childhood abuse without major depression (ELS/non-MDD), and women without a history of childhood abuse and major depression (non-ELS/MDD). Changes in neuroendocrine responses to CRF are correlated with psychological outcome measures. We hypothesize that treatment with fluoxetine will normalize altered neuroendocrine responsiveness in cases with ELS and that this normalization will be correlated with improvement of symptoms of depression and anxiety.


Criteria:

Inclusion Criteria: 1. For all subjects female gender; 2. For subjects assigned to the MDD groups, current DSM-IV diagnosis of MDD; 3. For subjects assigned to the early-life stress group, repeated (once per month or more for at least year) sexual or physical abuse before the age of 12 years by a perpetrator at least 5 years older at the time; 4. For all subjects, age of 18 to 45 years; 5. Regular menstrual cycle and assessment in the early follicular phase as verified by sex steroid measures. Exclusion Criteria: 1. For all subjects, gender identity disorders; 2. For all subjects assigned to non-MDD groups, DSM-IV diagnosis of current MDD; 3. For all subjects assigned to the group without early-life stress, major stress experiences before the age of 12 years, such as separation from parents, neglect, parental loss, accidents, severe illness or natural disaster; 4. For all subjects, significant medical illness, such as gastrointestinal, neurological, endocrine, cardiovascular, pulmonary, renal, hepatic, immunological or hematological disease, organic brain disease, or cancer as determined by history, physical examination, ECG, and laboratory tests; 5. Pregnancy or nursing; 6. For all subjects, past or current presence of psychotic symptoms or bipolar disorder; 7. For all subjects, current presence of psychoactive substance abuse/dependency or eating disorders; 8. For all subjects, hormonal medication; 9. For all subjects, psychotropic medication in the four weeks prior to study entry; 10. For all subjects, inability to provide informed consent.


NCT ID:

NCT00208897


Primary Contact:

Principal Investigator
Christine M Heim, PhD
Emory University-Dept. of Psychiatry and Behavioral Sciences


Backup Contact:

N/A


Location Contact:

Atlanta, Georgia 30322
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: April 03, 2020

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