Age
Item
ages between 18-65
boolean
C0001779 (UMLS CUI [1])
major depression, dysthymia or depression nos
Item
meets dsm-iv criteria for current major depression, dysthymia or depression nos
boolean
C1269683 (UMLS CUI [1])
C0013415 (UMLS CUI [2])
C0011581 (UMLS CUI [3])
hearing impairment
Item
known hearing impairment
boolean
C1384666 (UMLS CUI [1])
Suicidality
Item
active suicidal ideation (history of suicide attempts will be evaluated on a case by case basis)
boolean
C0438696 (UMLS CUI [1])
hamd
Item
hamd > 20
boolean
C0451203 (UMLS CUI [1])
alcohol and/or drug abuse or dependence
Item
current (past six months) alcohol and/or drug abuse or dependence
boolean
C0038586 (UMLS CUI [1])
medical condition contraindicated with study medication
Item
medical condition likely to require intervention contraindicated with study medication (e.g., known arrhythmia likely to be exacerbated by imipramine)
boolean
C0009488 (UMLS CUI [1])
bipolar i
Item
bipolar i
boolean
C0005586 (UMLS CUI [1])
C0853193 (UMLS CUI [2])
psychosis
Item
psychosis
boolean
C0033975 (UMLS CUI [1])
psychatric medication
Item
if currently taking antidepressants or mood stabilizers, cannot be off psychotropic medication for 7 weeks (10 weeks for prozac) or felt to require other psychiatric medication (other than occasional sleep or anxiety medication)
boolean
C0003289 (UMLS CUI [1])
C4020582 (UMLS CUI [2])
C0748066 (UMLS CUI [3])
birth control
Item
premenopausal women not using known effective birth control
boolean
C0700589 (UMLS CUI [1])
not currently depressed
Item
not currently depressed (whether considered due to current treatment or not)
boolean
C0344315 (UMLS CUI [1])
C0011570 (UMLS CUI [2])
response to treatment, escitalporam, imipramine
Item
nonresponse to adequate trial of both study medications (i.e., > 4weeks on > escitalopram 30 mg/d, and imipramine 200 mg/d); patients having an inadequate response to one study medication could be enrolled and receive the other; patients having responded to an adequate trial of either study medication would be offered a retrial; also excluded will be subjects having non responded to an adequate trial with citalopram (i.e., > 4 weeks on > citalopram 60 mg/d)
boolean
C0521982 (UMLS CUI [1])
C1099456 (UMLS CUI [2])
C0020934 (UMLS CUI [3])
left handed
Item
left-handed
boolean
C0234418 (UMLS CUI [1])