A 12-week placebo-controlled, randomized clinical trial was undertaken
to evaluate imipramine as a treatment for cocaine abuse, and to exami
ne whether its effect may be limited to subgroups defined by route of
use or by diagnosis of depression. One-hundred thirteen patients were
randomized, stratified by route of use and depression. All patients re
ceived weekly individual counseling. Compared to placebo the imipramin
e group showed greater reductions in cocaine craving, cocaine euphoria
, and depression, but the effect of imipramine on cocaine use was less
clear. A favorable response, defined as at least 3 consecutive, urine
-confirmed, cocaine-free weeks was achieved by 19% (11/59) of patients
on imipramine compared to 7% (4/54) on placebo (P < 0.09). The imipra
mine effect was greater among nasal users - 33% (9/27) response on imi
pramine vs. 5% (1/22) on placebo (P < 0.02). Response was also more fr
equent, but not significantly so, among depressed users on imipramine
(26%, 10/38) than on placebo (13%, 4/31) (P < 0.19). Response rates we
re low in intravenous and freebase users and those without depression.
Considered together with. the literature on desipramine, these data s
uggest tricyclic antidepressants are not promising as a mainstay of tr
eatment for unselected cocaine abusers, However, tricyclics may be use
ful for selected cocaine abusers with comorbid depression or intranasa
l use, or in conjunction with a more potent psychosocial intervention.