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Sponsored by: |
Sheba Medical Center |
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Information provided by: | Sheba Medical Center |
ClinicalTrials.gov Identifier: | NCT00429689 |
Subjects will be 1000 men meeting the following inclusion criteria: 1) male, age 18-65 years; 2) meeting DSM-IV criteria for major depressive disorder within the past one year, with a HAM-D score >12.
Subjects will be excluded if they exhibit 1) a substance abuse or dependence disorder within the past year; 2) current psychotic symptoms; or 3) a history of bipolar disorder.
Procedure
After informed consent, eligible patients will have blood drawn for serum hormone levels; cortisol, DHEA-S and tostestesterone or they will provide a salivary sample for measurement of hormone levels.
We will also test hormone level form 1000 healthy males (from blood or saliva) at the same age for comparison.
Condition | Intervention |
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Depression |
Procedure: Saliva sumple |
Study Type: | Observational |
Study Design: | Screening, Longitudinal, Defined Population, Retrospective Study |
Official Title: | Hormonal Levels in Men With Major Depressive Disorder |
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Male |
Inclusion Criteria:
Contact: Revital Amiaz, MD | +972-52-6666571 | revital.amiaz@sheba.health.gov.il |
Study Director: | Stuart Seidman,, MD | West End Medical Associates |
Principal Investigator: | Revital Amiaz, MD | Sheba Medical Center |
Study ID Numbers: | SHEBA-06-4480-RA-CTIL |
Study First Received: | January 31, 2007 |
Last Updated: | January 31, 2007 |
ClinicalTrials.gov Identifier: | NCT00429689 |
Health Authority: | Israel: The Israel National Institute for Health Policy Research and Health Services Research |
Male, MDD, Tostesterone, DHEA-S,Cortisol Male 18-65 Major Depression |
Hydrocortisone Depression Cortisol succinate Mental Disorders Mood Disorders |
Hydrocortisone acetate Depressive Disorder, Major Depressive Disorder Behavioral Symptoms |