Twenty-three premature ejaculators (PEs) and 11 control subjects were admin
istered 25 mg of clomipramine in a double-blind, placebo-controlled, crosso
ver design study. During 2-week trials, subjects took either the drug or th
e placebo 4 to 6 hours prior to sexual activity. Daily diary data revealed
that, for both groups, orgasmic latency was significantly increased when ta
king the clomipramine, For the PEs, the average increase in orgasmic latenc
y during intercourse was from less than 1 minute to more than 3.5 minutes.
Subjects also participated in two laboratory sessions while on the drug and
placebo, During these lab sessions they were exposed to erotic videos with
and without the addition of vibrotactile stimulation to the penis. Results
from the laboratory data support those from the diaries. Specifically, PEs
were significantly less likely to reach orgasm during the lab sessions whi
le on the clomipramine than while on the placebo. Further, they reported a
significantly greater sense of control over their orgasm while on the drug.
The results of this study, along with previous research, strongly support
the value of low doses of clomipramine in the treatment of premature ejacul
ation, specifically when taken on an as-needed basis as little as 4 hours p
rior to sexual activity. It is important to note, however, that the benefic
ial effects of the drag were not uniform across clinical subjects. In this
study, those PEs with the shortest orgasmic latencies while on the placebo
were the least likely to substantially improve while on the drug. Additiona
l research is necessary to determine whether changes in the timing and dosa
ge of the clomipramine administration can extend the benefits of the drug t
o those with the shortest latencies.